A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv594206



Internal ID16034929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:56907429..56909377hg38UCSC Ensembl
Innerchr4:57773595..57775543hg19UCSC Ensembl
Innerchr4:57468352..57470300hg18UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg381949
hg191949
hg181949
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv998042
Samples
Known GenesREST
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv594206
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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