A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565522



Internal ID16352931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:92414979..92461311hg38UCSC Ensembl
Innerchr14:92881323..92927655hg19UCSC Ensembl
Innerchr14:91951076..91997408hg18UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg3846333
hg1946333
hg1846333
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv832177
Samples
Known GenesSLC24A4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565522
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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