A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527432



Internal ID15454725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:123432809..123434768hg38UCSC Ensembl
Innerchr10:125192325..125194284hg19UCSC Ensembl
Innerchr10:125182315..125184274hg18UCSC Ensembl
Innerchr10:125182315..125184274hg17UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg381960
hg191960
hg181960
hg171960
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703871
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527432
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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