A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv691091



Internal ID15427743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:151279049..151307805hg38UCSC Ensembl
InnerchrX:150447521..150476277hg19UCSC Ensembl
InnerchrX:150198179..150226935hg18UCSC Ensembl
InnerchrX:150118089..150146845hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3828757
hg1928757
hg1828757
hg1728757
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517397
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv691091
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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