A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009697



Internal ID19098915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:197835164..197855907hg38UCSC Ensembl
Innerchr1:197804294..197825037hg19UCSC Ensembl
Innerchr1:196070917..196091660hg18UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg3820744
hg1920744
hg1820744
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3487510
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)nsv1009697
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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