A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608076



Internal ID6648315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:10521953..10552059hg38UCSC Ensembl
Innerchr6:10522453..10551559hg38UCSC Ensembl
Outerchr6:10520953..10553059hg38UCSC Ensembl
chr6:10522186..10552292hg19UCSC Ensembl
Innerchr6:10522686..10551792hg19UCSC Ensembl
Outerchr6:10521186..10553292hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg3830107
hg1930107
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1165e214
Supporting Variantsessv12188403, essv12188404
SamplesHG03857, HG00611
Known GenesGCNT2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608076
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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