A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017742



Internal ID19106959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:9804499..9947062hg38UCSC Ensembl
Innerchr6:9804732..9947295hg19UCSC Ensembl
Innerchr6:9912718..10055281hg18UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg38142564
hg19142564
hg18142564
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5916n100
Supporting Variantsnssv3654759
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)nsv1017742
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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