A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024485



Internal ID19113702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:116735282..116751528hg38UCSC Ensembl
Innerchr7:116375336..116391582hg19UCSC Ensembl
Innerchr7:116162572..116178818hg18UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg3816247
hg1916247
hg1816247
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3662050
Samples
Known GenesMET
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024485
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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