A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1100254



Internal ID15953440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:154881129..154909643hg38UCSC Ensembl
Innerchr7:154672839..154701353hg19UCSC Ensembl
Innerchr7:154303772..154332286hg18UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg3828515
hg1928515
hg1828515
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv609115
Supporting Variants
Samples
Known GenesDPP6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1100254
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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