A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6390931



Internal ID21048484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:62960405..64322157hg38UCSC Ensembl
chr4:63826123..65187875hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg381361753
hg191361753
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5286n223
Supporting Variantsnssv18119250
Samples
Known GenesTECRL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6390931
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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