A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608943



Internal ID20982014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:24572401..24574500hg38UCSC Ensembl
chr7:24612020..24614119hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234997
Samples
Known GenesMPP6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608943
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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