A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6321n100



Internal ID20157937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:35898674..35977765hg38UCSC Ensembl
chr7:35938284..36017375hg19UCSC Ensembl
chr7:35904809..35983900hg18UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg3879092
hg1979092
hg1879092
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1023070, nsv1028202, nsv1023464, nsv1022680
Samples
Known GenesSEPT7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6321n100
Frequency
Sample Size29084
Observed Gain14
Observed Loss0
Observed Complex0
Frequencyn/a


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