A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020449



Internal ID18762984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:150856657..150875482hg38UCSC Ensembl
Innerchr7:150553745..150572570hg19UCSC Ensembl
Innerchr7:150184678..150203503hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3818826
hg1918826
hg1818826
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6755n100
Supporting Variantsnssv3674263, nssv3674264, nssv3757723, nssv3757722
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)nsv1020449
Frequency
Sample Size29084
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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