A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550672



Internal ID15991395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:42257742..42946281hg38UCSC Ensembl
Innerchr10:42753190..43441729hg19UCSC Ensembl
Innerchr10:42073196..42761735hg18UCSC Ensembl
Cytoband10q11.1
Allele length
AssemblyAllele length
hg38688540
hg19688540
hg18688540
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv747290
Samples
Known GenesBMS1, CCNYL2, LINC00839, LOC441666, ZNF33B, ZNF37BP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550672
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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