A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549997



Internal ID15990720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:14459237..14814109hg38UCSC Ensembl
Innerchr10:14501236..14856108hg19UCSC Ensembl
Innerchr10:14541242..14896114hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38354873
hg19354873
hg18354873
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv744077
Samples
Known GenesFAM107B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549997
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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