A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517977



Internal ID15445270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:144392048..144410097hg38UCSC Ensembl
InnerchrX:143475142..143493192hg19UCSC Ensembl
InnerchrX:143302828..143320878hg18UCSC Ensembl
InnerchrX:143200682..143218732hg17UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg3818050
hg1918051
hg1818051
hg1718051
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695389
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517977
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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