A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705594



Internal ID15442246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:155138143..155217482hg38UCSC Ensembl
InnerchrX:154366418..154445759hg19UCSC Ensembl
InnerchrX:154019612..154098953hg18UCSC Ensembl
InnerchrX:153930122..154009463hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3879340
hg1979342
hg1879342
hg1779342
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528909
Supporting Variants
Samples
Known GenesVBP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705594
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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