A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525994



Internal ID15453287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:35577155..35600108hg38UCSC Ensembl
Innerchr5:35577257..35600210hg19UCSC Ensembl
Innerchr5:35613014..35635967hg18UCSC Ensembl
Innerchr5:35613014..35635967hg17UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg3822954
hg1922954
hg1822954
hg1722954
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702219
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525994
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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