A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694104



Internal ID15430756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:45210714..45230374hg38UCSC Ensembl
InnerchrX:45069959..45089619hg19UCSC Ensembl
InnerchrX:44954903..44974563hg18UCSC Ensembl
InnerchrX:44826213..44845873hg17UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg3819661
hg1919661
hg1819661
hg1719661
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521851
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694104
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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