A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv665946



Internal ID15402598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:123804679..123832142hg38UCSC Ensembl
InnerchrX:122938529..122965992hg19UCSC Ensembl
InnerchrX:122766210..122793673hg18UCSC Ensembl
InnerchrX:122664064..122691527hg17UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg3827464
hg1927464
hg1827464
hg1727464
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517283
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv665946
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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