A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620483



Internal ID7007354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:42770480..42812210hg38UCSC Ensembl
chr9:44158909..44200752hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3841731
hg1941844
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13482442, essv13482449, essv13482440, essv13482447, essv13482439, essv13482445, essv13482443, essv13482448, essv13482444, essv13482446, essv13482441, essv13482438
SamplesHG01054, HG02262, NA12058, HG00641, HG02703, NA19189, HG01603, NA19707, HG03713, HG02546, HG01111, NA18740
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620483
Frequency
Sample Size2504
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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