A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550775



Internal ID15991498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46224041..46279254hg38UCSC Ensembl
Innerchr10:47595277..47650490hg19UCSC Ensembl
Innerchr10:47065283..47120496hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3855214
hg1955214
hg1855214
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174506, nssv1174507, nssv1174508
SamplesNINDS_197, NINDS_102, NINDS_44
Known GenesANTXRLP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550775
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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