A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027849



Internal ID19117067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:19963471..20045375hg38UCSC Ensembl
Innerchr7:20003094..20084998hg19UCSC Ensembl
Innerchr7:19969619..20051523hg18UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3881905
hg1981905
hg1881905
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3643263
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1027849
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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