A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18234997



Internal ID20802037
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 StatusS
Merged Variantsnsv6608943
Supporting Variants
Samples
Known GenesMPP6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18234997
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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