A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv672973



Internal ID15409625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:144663617..144726602hg38UCSC Ensembl
InnerchrX:143745138..143808123hg19UCSC Ensembl
InnerchrX:143552719..143615817hg18UCSC Ensembl
InnerchrX:143450573..143513671hg17UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg3862986
hg1962986
hg1863099
hg1763099
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516515
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv672973
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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