A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003096



Internal ID19092313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:188112830..188268035hg38UCSC Ensembl
Innerchr1:188081961..188237166hg19UCSC Ensembl
Innerchr1:186348584..186503789hg18UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg38155206
hg19155206
hg18155206
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3488084
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)nsv1003096
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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