A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6381556



Internal ID21039109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:160265837..160278087hg38UCSC Ensembl
chr4:161186989..161199239hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3812251
hg1912251
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18112944
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6381556
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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