A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696940



Internal ID15433592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:43555801..43558623hg38UCSC Ensembl
Innerchr7:43595400..43598222hg19UCSC Ensembl
Innerchr7:43561925..43564747hg18UCSC Ensembl
Innerchr7:43368640..43371462hg17UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg382823
hg192823
hg182823
hg172823
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519592
Supporting Variants
Samples
Known GenesHECW1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696940
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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