A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1093602



Internal ID15600102
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 StatusS
Merged Variantsnsv608341
Supporting Variants
Samples
Known GenesPOT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1093602
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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