A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699031



Internal ID15435683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:28068379..28196103hg38UCSC Ensembl
InnerchrX:28086496..28214220hg19UCSC Ensembl
InnerchrX:27996417..28124141hg18UCSC Ensembl
InnerchrX:27846153..27973877hg17UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg38127725
hg19127725
hg18127725
hg17127725
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523291
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699031
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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