A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526913



Internal ID15107520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:97729477..97776258hg38UCSC Ensembl
Innerchr8:98741705..98788486hg19UCSC Ensembl
Innerchr8:98810881..98857662hg18UCSC Ensembl
Innerchr8:98810881..98857662hg17UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3846782
hg1946782
hg1846782
hg1746782
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703274
Samples
Known GenesLAPTM4B, MTDH
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526913
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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