A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606748



Internal ID16394157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:44107701..44113786hg38UCSC Ensembl
Innerchr7:44147300..44153385hg19UCSC Ensembl
Innerchr7:44113825..44119910hg18UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg386086
hg196086
hg186086
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11297n54
Supporting Variantsnssv1083227
Samples
Known GenesAEBP1, MIR4649
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606748
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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