A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv656380



Internal ID15393032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:45293418..45382702hg38UCSC Ensembl
InnerchrX:45152663..45241947hg19UCSC Ensembl
InnerchrX:45037607..45126891hg18UCSC Ensembl
InnerchrX:44908917..44998201hg17UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg3889285
hg1989285
hg1889285
hg1789285
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519486
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv656380
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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