A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549996



Internal ID15990719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:13964391..14242607hg38UCSC Ensembl
Innerchr10:14006391..14284606hg19UCSC Ensembl
Innerchr10:14046397..14324612hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38278217
hg19278216
hg18278216
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv744076
Samples
Known GenesFRMD4A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549996
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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