A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6377556



Internal ID21035109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:96960359..96961253hg38UCSC Ensembl
chr4:97881510..97882404hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg38895
hg19895
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18121454
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6377556
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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