A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697321



Internal ID15433973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:151289462..151302884hg38UCSC Ensembl
InnerchrX:150457934..150471356hg19UCSC Ensembl
InnerchrX:150208592..150222014hg18UCSC Ensembl
InnerchrX:150128502..150141924hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3813423
hg1913423
hg1813423
hg1713423
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)nssv697321
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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