A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv690753



Internal ID15427405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46257656..46279254hg38UCSC Ensembl
Innerchr10:47628892..47650490hg19UCSC Ensembl
Innerchr10:47098898..47120496hg18UCSC Ensembl
Innerchr10:47098898..47120496hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3821599
hg1921599
hg1821599
hg1721599
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516485
Supporting Variants
Samples
Known GenesANTXRLP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv690753
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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