A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv685703



Internal ID15422355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:144663617..144740259hg38UCSC Ensembl
InnerchrX:143745138..143821780hg19UCSC Ensembl
InnerchrX:143552719..143629479hg18UCSC Ensembl
InnerchrX:143450573..143527333hg17UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg3876643
hg1976643
hg1876761
hg1776761
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)nssv685703
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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