A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699135



Internal ID15089101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:148473389..148517170hg38UCSC Ensembl
InnerchrX:147554909..147598691hg19UCSC Ensembl
InnerchrX:147362601..147406383hg18UCSC Ensembl
InnerchrX:147260455..147304237hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3843782
hg1943783
hg1843783
hg1743783
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523386
Supporting Variants
Samples
Known GenesAFF2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699135
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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