A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6754n100



Internal ID20158370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:150850025..150877464hg38UCSC Ensembl
chr7:150547113..150574552hg19UCSC Ensembl
chr7:150178046..150205485hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3827440
hg1927440
hg1827440
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1029395, nsv1031497
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)dgv6754n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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