A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022811



Internal ID19112029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:154320960..154378386hg38UCSC Ensembl
Innerchr7:154018045..154075471hg19UCSC Ensembl
Innerchr7:153648978..153706404hg18UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg3857427
hg1957427
hg1857427
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3674660
Samples
Known GenesDPP6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022811
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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