A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004106



Internal ID19093323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:195861190..195906930hg38UCSC Ensembl
Innerchr1:195830320..195876060hg19UCSC Ensembl
Innerchr1:194096943..194142683hg18UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg3845741
hg1945741
hg1845741
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv502n100
Supporting Variantsnssv3487640
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)nsv1004106
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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