A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608441



Internal ID16395850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:133418294..133540655hg38UCSC Ensembl
Innerchr7:133103048..133225409hg19UCSC Ensembl
Innerchr7:132753588..132875949hg18UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38122362
hg19122362
hg18122362
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1155233
SamplesNINDS_229
Known GenesEXOC4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608441
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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