A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702530



Internal ID15439182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:33391678..33539786hg38UCSC Ensembl
InnerchrX:33409795..33557903hg19UCSC Ensembl
InnerchrX:33319716..33467824hg18UCSC Ensembl
InnerchrX:33169452..33317560hg17UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg38148109
hg19148109
hg18148109
hg17148109
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526258
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702530
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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