A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6021n100



Internal ID22792108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:76726430..76759367hg38UCSC Ensembl
chr6:77436147..77469084hg19UCSC Ensembl
chr6:77492866..77525803hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3832938
hg1932938
hg1832938
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1017724, nsv1030490, nsv1031654, nsv1028754, nsv1029002, nsv1023909, nsv1026686
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)dgv6021n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss25
Observed Complex0
Frequencyn/a


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