A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515977



Internal ID15096584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:88673046..88708284hg38UCSC Ensembl
Innerchr5:87968864..88004101hg19UCSC Ensembl
Innerchr5:88004620..88039857hg18UCSC Ensembl
Innerchr5:88004620..88039857hg17UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3835239
hg1935238
hg1835238
hg1735238
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv669567, nssv665567, nssv692763, nssv669813, nssv696769, nssv668740, nssv658392, nssv667297, nssv705358
Samples
Known GenesLINC00461
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515977
Frequency
Sample Size2026
Observed Gain1
Observed Loss8
Observed Complex0
Frequencyn/a


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