A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623073



Internal ID6663241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:44841203..44842031hg38UCSC Ensembl
Innerchr10:44841221..44842014hg38UCSC Ensembl
Outerchr10:44841186..44842049hg38UCSC Ensembl
chr10:45336651..45337479hg19UCSC Ensembl
Innerchr10:45336669..45337462hg19UCSC Ensembl
Outerchr10:45336634..45337497hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38829
hg19829
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13765106, essv13765110, essv13765107, essv13765102, essv13765116, essv13765108, essv13765113, essv13765101, essv13765115, essv13765104, essv13765117, essv13765112, essv13765103, essv13765111, essv13765109, essv13765114, essv13765105, essv13765100
SamplesHG02583, NA19909, HG03280, HG02476, HG03074, HG03464, HG03209, HG02885, HG02820, NA19184, HG02511, HG03081, HG02878, HG01101, HG03064, NA06986, HG03039, NA18505
Known GenesTMEM72-AS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623073
Frequency
Sample Size2504
Observed Gain0
Observed Loss18
Observed Complex0
Frequencyn/a


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