A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv670218



Internal ID15406870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:93337360..93461201hg38UCSC Ensembl
InnerchrX:92592359..92716200hg19UCSC Ensembl
InnerchrX:92479015..92602856hg18UCSC Ensembl
InnerchrX:92398504..92522345hg17UCSC Ensembl
CytobandXq21.32
Allele length
AssemblyAllele length
hg38123842
hg19123842
hg18123842
hg17123842
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516563
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv670218
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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