A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv654397



Internal ID15391049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:112237770..112379276hg38UCSC Ensembl
InnerchrX:111480998..111622504hg19UCSC Ensembl
InnerchrX:111367654..111509160hg18UCSC Ensembl
InnerchrX:111287143..111428649hg17UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38141507
hg19141507
hg18141507
hg17141507
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516845
Supporting Variants
Samples
Known GenesZCCHC16
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv654397
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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