A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6381714



Internal ID21039267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:159362242..159393554hg38UCSC Ensembl
chr4:160283394..160314706hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3831313
hg1931313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18111720
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6381714
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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