A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv673645



Internal ID15410297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:112258052..112401274hg38UCSC Ensembl
InnerchrX:111501280..111644502hg19UCSC Ensembl
InnerchrX:111387936..111531158hg18UCSC Ensembl
InnerchrX:111307425..111450647hg17UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38143223
hg19143223
hg18143223
hg17143223
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)nssv673645
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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