A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6395617



Internal ID21053170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:65919001..65983300hg38UCSC Ensembl
chr5:65214829..65279128hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg3864300
hg1964300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214834
Samples
Known GenesERBB2IP, LOC100303749
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6395617
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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