A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516188



Internal ID15443481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:184471845..184476400hg38UCSC Ensembl
Innerchr3:184189633..184194188hg19UCSC Ensembl
Innerchr3:185672327..185676882hg18UCSC Ensembl
Innerchr3:185672335..185676890hg17UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg384556
hg194556
hg184556
hg174556
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv672141, nssv666677, nssv681199, nssv696600, nssv678969, nssv681913, nssv667180, nssv658153
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516188
Frequency
Sample Size2026
Observed Gain1
Observed Loss7
Observed Complex0
Frequencyn/a


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