A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704080



Internal ID15440732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:49373037..49383154hg38UCSC Ensembl
Innerchr7:49412633..49422750hg19UCSC Ensembl
Innerchr7:49383179..49393296hg18UCSC Ensembl
Innerchr7:49189894..49200011hg17UCSC Ensembl
Cytoband7p12.2
Allele length
AssemblyAllele length
hg3810118
hg1910118
hg1810118
hg1710118
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515884
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704080
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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