A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6380936



Internal ID21038489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:56072759..56193475hg38UCSC Ensembl
chr4:56938925..57059641hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38120717
hg19120717
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18118401
Samples
Known GenesKIAA1211
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6380936
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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