A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608874



Internal ID20981945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:50090901..50096500hg38UCSC Ensembl
chr7:50130497..50136096hg19UCSC Ensembl
Cytoband7p12.2
Allele length
AssemblyAllele length
hg385600
hg195600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6665n223
Supporting Variantsnssv18233851
Samples
Known GenesC7orf72, ZPBP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608874
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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