A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699929



Internal ID15436581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:152087024..152095548hg38UCSC Ensembl
InnerchrX:151255496..151264020hg19UCSC Ensembl
InnerchrX:151006152..151014676hg18UCSC Ensembl
InnerchrX:150926064..150934588hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg388525
hg198525
hg188525
hg178525
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517791
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699929
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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