A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703465



Internal ID15440117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:88397486..88424986hg38UCSC Ensembl
InnerchrX:87652487..87679987hg19UCSC Ensembl
InnerchrX:87539143..87566643hg18UCSC Ensembl
InnerchrX:87458632..87486132hg17UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg3827501
hg1927501
hg1827501
hg1727501
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527086
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703465
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer