A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv667336



Internal ID15403988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:44725861..44795709hg38UCSC Ensembl
InnerchrX:44585107..44654955hg19UCSC Ensembl
InnerchrX:44470051..44539899hg18UCSC Ensembl
InnerchrX:44341361..44411209hg17UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg3869849
hg1969849
hg1869849
hg1769849
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516286
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv667336
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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