A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016340



Internal ID19105559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:86076942..86148453hg38UCSC Ensembl
Innerchr7:85706258..85777769hg19UCSC Ensembl
Innerchr7:85544194..85615705hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3871512
hg1971512
hg1871512
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655184
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)nsv1016340
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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