A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024708



Internal ID19113925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:98099939..98200359hg38UCSC Ensembl
Innerchr6:98547815..98648235hg19UCSC Ensembl
Innerchr6:98654536..98754956hg18UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38100421
hg19100421
hg18100421
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6111n100
Supporting Variantsnssv3649844, nssv3649845
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)nsv1024708
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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