A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6712n100



Internal ID20158328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:143733483..143897882hg38UCSC Ensembl
chr7:143430576..143594975hg19UCSC Ensembl
chr7:143061509..143225908hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38164400
hg19164400
hg18164400
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1015415, nsv1024467, nsv1023202, nsv1030567, nsv1034767, nsv1024496, nsv1019581, nsv1020550
Samples
Known GenesCTAGE6, FAM115A, LOC154761
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6712n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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