A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524643



Internal ID15451936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:2169843..2177736hg38UCSC Ensembl
Innerchr10:2212037..2219930hg19UCSC Ensembl
Innerchr10:2202037..2209930hg18UCSC Ensembl
Innerchr10:2202037..2209930hg17UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg387894
hg197894
hg187894
hg177894
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700609
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524643
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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