A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608439



Internal ID16395848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:132201167..132215596hg38UCSC Ensembl
Innerchr7:131885926..131900355hg19UCSC Ensembl
Innerchr7:131536466..131550895hg18UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg3814430
hg1914430
hg1814430
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1094543
Samples
Known GenesPLXNA4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608439
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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