A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516871



Internal ID15097478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:71833693..72033254hg38UCSC Ensembl
Innerchr15:72126034..72325595hg19UCSC Ensembl
Innerchr15:69913088..70112649hg18UCSC Ensembl
Innerchr15:69913088..70112649hg17UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38199562
hg19199562
hg18199562
hg17199562
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv658146, nssv696349, nssv654609, nssv694825, nssv702292, nssv692778
Samples
Known GenesMYO9A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516871
Frequency
Sample Size2026
Observed Gain1
Observed Loss5
Observed Complex0
Frequencyn/a


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