A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv682509



Internal ID15072475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:71888508..71924255hg38UCSC Ensembl
InnerchrX:71108358..71144105hg19UCSC Ensembl
InnerchrX:71025083..71060830hg18UCSC Ensembl
InnerchrX:70891379..70927126hg17UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg3835748
hg1935748
hg1835748
hg1735748
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517419
Supporting Variants
Samples
Known GenesNHSL2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv682509
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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