A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6385240



Internal ID21042793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:70952560..70964847hg38UCSC Ensembl
chr4:71818277..71830564hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg3812288
hg1912288
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18120049
Samples
Known GenesMOB1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6385240
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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