A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv672582



Internal ID15062548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:103933493..104034456hg38UCSC Ensembl
InnerchrX:103188067..103289019hg19UCSC Ensembl
InnerchrX:103074723..103175675hg18UCSC Ensembl
InnerchrX:102994212..103095164hg17UCSC Ensembl
CytobandXq22.2
Allele length
AssemblyAllele length
hg38100964
hg19100953
hg18100953
hg17100953
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519626
Supporting Variants
Samples
Known GenesH2BFWT, H2BFXP, MIR1256, TMSB15B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv672582
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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