A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6755n100



Internal ID20158371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:150855785..150875482hg38UCSC Ensembl
chr7:150552873..150572570hg19UCSC Ensembl
chr7:150183806..150203503hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3819698
hg1919698
hg1819698
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1020449, nsv1028241
Samples
Known GenesAOC1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6755n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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