A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6379018



Internal ID21036571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:175955622..175970880hg38UCSC Ensembl
chr4:176876773..176892031hg19UCSC Ensembl
Cytoband4q34.2
Allele length
AssemblyAllele length
hg3815259
hg1915259
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212781
Samples
Known GenesGPM6A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6379018
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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