A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604162



Internal ID16391571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:93227679..93268190hg38UCSC Ensembl
Innerchr6:93937397..93977908hg19UCSC Ensembl
Innerchr6:93994118..94034629hg18UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3840512
hg1940512
hg1840512
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1068418
Samples
Known GenesEPHA7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604162
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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