A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5917n100



Internal ID20157533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:10465938..10535418hg38UCSC Ensembl
chr6:10466171..10535651hg19UCSC Ensembl
chr6:10574157..10643637hg18UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg3869481
hg1969481
hg1869481
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1028517, nsv1020564, nsv1029884, nsv1023163, nsv1025443, nsv1018041, nsv1018322, nsv1018741
Samples
Known GenesGCNT2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5917n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss27
Observed Complex0
Frequencyn/a


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