A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv656083



Internal ID15392735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:44725861..44755902hg38UCSC Ensembl
InnerchrX:44585107..44615148hg19UCSC Ensembl
InnerchrX:44470051..44500092hg18UCSC Ensembl
InnerchrX:44341361..44371402hg17UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg3830042
hg1930042
hg1830042
hg1730042
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)nssv656083
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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