A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701872



Internal ID15438524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:69236982..69252984hg38UCSC Ensembl
InnerchrX:68456825..68472827hg19UCSC Ensembl
InnerchrX:68373550..68389552hg18UCSC Ensembl
InnerchrX:68239846..68255848hg17UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg3816003
hg1916003
hg1816003
hg1716003
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525710
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701872
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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