A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5915n100



Internal ID22792002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:8589683..8722484hg38UCSC Ensembl
chr6:8589916..8722717hg19UCSC Ensembl
chr6:8534915..8667716hg18UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg38132802
hg19132802
hg18132802
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1022625, nsv1017541
Samples
Known GenesHULC, LOC100506207
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5915n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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