A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv669180



Internal ID15405832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:93267146..93426754hg38UCSC Ensembl
InnerchrX:92522145..92681753hg19UCSC Ensembl
InnerchrX:92408801..92568409hg18UCSC Ensembl
InnerchrX:92328290..92487898hg17UCSC Ensembl
CytobandXq21.32
Allele length
AssemblyAllele length
hg38159609
hg19159609
hg18159609
hg17159609
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516563
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv669180
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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