A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702040



Internal ID15092006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:152434786..152511752hg38UCSC Ensembl
InnerchrX:151603258..151680224hg19UCSC Ensembl
InnerchrX:151353914..151430880hg18UCSC Ensembl
InnerchrX:151273826..151350792hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3876967
hg1976967
hg1876967
hg1776967
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516934
Supporting Variants
Samples
Known GenesGABRA3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702040
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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