A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694173



Internal ID15430825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:54599382..54603241hg38UCSC Ensembl
InnerchrX:54625815..54629674hg19UCSC Ensembl
InnerchrX:54642540..54646399hg18UCSC Ensembl
InnerchrX:54508836..54512695hg17UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg383860
hg193860
hg183860
hg173860
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517375
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694173
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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