A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524726



Internal ID15452019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:141945565..142045694hg38UCSC Ensembl
InnerchrX:141033351..141133480hg19UCSC Ensembl
InnerchrX:140861017..140961146hg18UCSC Ensembl
InnerchrX:140758871..140859000hg17UCSC Ensembl
CytobandXq27.2
Allele length
AssemblyAllele length
hg38100130
hg19100130
hg18100130
hg17100130
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700714
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524726
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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