A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704079



Internal ID15440731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:22644003..22651395hg38UCSC Ensembl
Innerchr7:22683622..22691014hg19UCSC Ensembl
Innerchr7:22650147..22657539hg18UCSC Ensembl
Innerchr7:22456862..22464254hg17UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg387393
hg197393
hg187393
hg177393
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527614
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704079
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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