A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033064



Internal ID19122286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:107262654..107309195hg38UCSC Ensembl
Innerchr7:106903099..106949640hg19UCSC Ensembl
Innerchr7:106690335..106736876hg18UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg3846542
hg1946542
hg1846542
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3755479
Samples
Known GenesCOG5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033064
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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