A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516845



Internal ID15444138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:112237770..112401274hg38UCSC Ensembl
InnerchrX:111480998..111644502hg19UCSC Ensembl
InnerchrX:111367654..111531158hg18UCSC Ensembl
InnerchrX:111287143..111450647hg17UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38163505
hg19163505
hg18163505
hg17163505
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697611, nssv654397, nssv658812, nssv697855, nssv698960, nssv673645
Samples
Known GenesZCCHC16
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516845
Frequency
Sample Size2026
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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