A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6709n100



Internal ID22792796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:143728285..143833864hg38UCSC Ensembl
chr7:143425378..143530957hg19UCSC Ensembl
chr7:143056311..143161890hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38105580
hg19105580
hg18105580
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1017891, nsv1020084, nsv1018338, nsv1016158, nsv1033245, nsv1028400
Samples
Known GenesCTAGE6, FAM115C, LOC154761
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6709n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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