A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019542



Internal ID19108760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:84533348..84571499hg38UCSC Ensembl
Innerchr7:84162664..84200815hg19UCSC Ensembl
Innerchr7:84000600..84038751hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3838152
hg1938152
hg1838152
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655163
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019542
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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