A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030100



Internal ID19119319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:76292716..76318052hg38UCSC Ensembl
Innerchr6:77002433..77027769hg19UCSC Ensembl
Innerchr6:77059153..77084489hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3825337
hg1925337
hg1825337
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6017n100
Supporting Variantsnssv3747085
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)nsv1030100
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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