A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699938



Internal ID15436590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:13214714..13234288hg38UCSC Ensembl
InnerchrX:13232833..13252407hg19UCSC Ensembl
InnerchrX:13142754..13162328hg18UCSC Ensembl
InnerchrX:12992490..13012064hg17UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg3819575
hg1919575
hg1819575
hg1719575
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524070
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699938
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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