A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211609



Internal ID20778649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:6611965..6627744hg38UCSC Ensembl
chr4:6613692..6629471hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3815780
hg1915780
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6371238
Supporting Variants
Samples
Known GenesMAN2B2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211609
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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