A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019640



Internal ID19108858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:104173074..104244257hg38UCSC Ensembl
Innerchr7:103813522..103884705hg19UCSC Ensembl
Innerchr7:103600758..103671941hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3871184
hg1971184
hg1871184
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6544n100
Supporting Variantsnssv3656129
Samples
Known GenesORC5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019640
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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