A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18196018



Internal ID20763058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:94835601..94869700hg38UCSC Ensembl
chr15:95378830..95412929hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3834100
hg1934100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6502859
Supporting Variants
Samples
Known GenesLOC440311
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18196018
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00069


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