A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515667



Internal ID15443278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:66292519..66299570hg38UCSC Ensembl
Innerchr17:64288637..64295688hg19UCSC Ensembl
Innerchr17:61719099..61726150hg18UCSC Ensembl
Innerchr17:61719099..61726150hg17UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg387052
hg197052
hg187052
hg177052
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv664654, nssv669318, nssv658066, nssv664312, nssv667397, nssv684275, nssv693692, nssv668293, nssv682399, nssv695512, nssv680857, nssv665267, nssv668309, nssv670958
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515667
Frequency
Sample Size2026
Observed Gain1
Observed Loss13
Observed Complex0
Frequencyn/a


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