A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv681846



Internal ID15071812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:97776033..97776258hg38UCSC Ensembl
Innerchr8:98788261..98788486hg19UCSC Ensembl
Innerchr8:98857437..98857662hg18UCSC Ensembl
Innerchr8:98857437..98857662hg17UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38226
hg19226
hg18226
hg17226
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517493
Supporting Variants
Samples
Known GenesLAPTM4B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv681846
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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