A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18235115



Internal ID20802155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:50496899..50713944hg38UCSC Ensembl
chr7:50564597..50781641hg19UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg38217046
hg19217045
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6617509
Supporting Variants
Samples
Known GenesDDC, GRB10, LOC100129427
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18235115
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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