A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516470



Internal ID15443763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:84773881..84775615hg38UCSC Ensembl
Innerchr1:85239564..85241298hg19UCSC Ensembl
Innerchr1:85012152..85013886hg18UCSC Ensembl
Innerchr1:84951585..84953319hg17UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg381735
hg191735
hg181735
hg171735
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv686856, nssv690492, nssv658797, nssv668576, nssv704475
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516470
Frequency
Sample Size2026
Observed Gain1
Observed Loss4
Observed Complex0
Frequencyn/a


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