A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608341



Internal ID16049064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:124846926..124932234hg38UCSC Ensembl
Innerchr7:124486980..124572288hg19UCSC Ensembl
Innerchr7:124274216..124359524hg18UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg3885309
hg1985309
hg1885309
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1093602
Samples
Known GenesPOT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608341
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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