A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620624



Internal ID7007494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:72064302..72069353hg38UCSC Ensembl
Innerchr9:72064302..72069353hg38UCSC Ensembl
Outerchr9:72064055..72069452hg38UCSC Ensembl
chr9:74679218..74684269hg19UCSC Ensembl
Innerchr9:74679218..74684269hg19UCSC Ensembl
Outerchr9:74678971..74684368hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg385052
hg195052
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13515782, essv13515775, essv13515785, essv13515780, essv13515777, essv13515784, essv13515783, essv13515776, essv13515779, essv13515774, essv13515773, essv13515772, essv13515781, essv13515778, essv13515786
SamplesNA12842, HG01305, NA18878, NA12340, HG01058, HG02449, NA12718, HG01047, NA19449, HG01197, NA19031, NA19390, NA19435, NA19324, HG01108
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620624
Frequency
Sample Size2504
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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