A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv609208



Internal ID16396617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:156596652..156611368hg38UCSC Ensembl
Innerchr7:156389346..156404062hg19UCSC Ensembl
Innerchr7:156082107..156096823hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3814717
hg1914717
hg1814717
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11759n54
Supporting Variantsnssv1100518, nssv1100517
Samples
Known GenesLINC01006
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv609208
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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