A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697088



Internal ID15433740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:113004993..113128595hg38UCSC Ensembl
InnerchrX:112248221..112371823hg19UCSC Ensembl
InnerchrX:112134877..112258479hg18UCSC Ensembl
InnerchrX:112054366..112177968hg17UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38123603
hg19123603
hg18123603
hg17123603
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519856
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697088
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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