A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367250



Internal ID21024803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:16333426..16382385hg38UCSC Ensembl
chr4:16335049..16384008hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3848960
hg1948960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18113770
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367250
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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