A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611386



Internal ID6998295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:157925184..157925937hg38UCSC Ensembl
Innerchr6:157925270..157925710hg38UCSC Ensembl
Outerchr6:157924964..157926157hg38UCSC Ensembl
chr6:158346216..158346969hg19UCSC Ensembl
Innerchr6:158346302..158346742hg19UCSC Ensembl
Outerchr6:158345996..158347189hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38754
hg19754
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12604961, essv12604950, essv12604954, essv12604951, essv12604948, essv12604960, essv12604955, essv12604972, essv12604968, essv12604965, essv12604964, essv12604956, essv12604957, essv12604962, essv12604959, essv12604970, essv12604971, essv12604947, essv12604973, essv12604953, essv12604952, essv12604969, essv12604958, essv12604949, essv12604966, essv12604967, essv12604963
SamplesHG02583, NA18508, HG02852, HG02798, NA19350, HG03521, HG03297, HG02888, NA19448, HG03578, NA19130, HG02715, NA19908, NA18934, NA19175, HG03575, HG03081, HG02283, NA19338, NA18523, HG02635, HG01896, NA19321, NA19434, HG02982, HG02938, NA19214
Known GenesSNX9
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611386
Frequency
Sample Size2504
Observed Gain0
Observed Loss27
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer