A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029201



Internal ID19118420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:98099939..98204719hg38UCSC Ensembl
Innerchr6:98547815..98652595hg19UCSC Ensembl
Innerchr6:98654536..98759316hg18UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38104781
hg19104781
hg18104781
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6111n100
Supporting Variantsnssv3649846
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)nsv1029201
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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