A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891069



Internal ID19185465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:16094088..16118136hg38UCSC Ensembl
Outerchr7:16094088..16118136hg38UCSC Ensembl
Innerchr7:16133713..16157761hg19UCSC Ensembl
Outerchr7:16133713..16157761hg19UCSC Ensembl
Innerchr7:16100238..16124286hg18UCSC Ensembl
Outerchr7:16100238..16124286hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3824049
hg1924049
hg1824049
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25781379
Samples
Known GenesISPD
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891069
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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