A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1078469



Internal ID15584969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:2516523..2540436hg38UCSC Ensembl
Innerchr7:2556157..2580070hg19UCSC Ensembl
Innerchr7:2522683..2546596hg18UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg3823914
hg1923914
hg1823914
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605861
Supporting Variants
Samples
Known GenesBRAT1, LFNG, MIR4648
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1078469
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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