A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6096n100



Internal ID22792183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:94445384..94606013hg38UCSC Ensembl
chr6:95155102..95315731hg19UCSC Ensembl
chr6:95211823..95372452hg18UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38160630
hg19160630
hg18160630
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1025326, nsv1026738
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)dgv6096n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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