A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025144



Internal ID18767676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:80567970..80642525hg38UCSC Ensembl
Innerchr7:80197286..80271841hg19UCSC Ensembl
Innerchr7:80035222..80109777hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3874556
hg1974556
hg1874556
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655138
Samples
Known GenesCD36
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1025144
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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