A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007919



Internal ID19097138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:191312186..191653300hg38UCSC Ensembl
Innerchr1:191281316..191622430hg19UCSC Ensembl
Innerchr1:189547939..189889053hg18UCSC Ensembl
Cytoband1q31.2
Allele length
AssemblyAllele length
hg38341115
hg19341115
hg18341115
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3494679
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)nsv1007919
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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