A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515717



Internal ID15443328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:6691940..6699111hg38UCSC Ensembl
Innerchr5:6692053..6699224hg19UCSC Ensembl
Innerchr5:6745053..6752224hg18UCSC Ensembl
Innerchr5:6745053..6752224hg17UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg387172
hg197172
hg187172
hg177172
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv664538, nssv659946, nssv705599, nssv658290, nssv660083, nssv671009, nssv667184, nssv672969, nssv661234
Samples
Known GenesLOC100505625
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515717
Frequency
Sample Size2026
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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