A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6386901



Internal ID21044454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:56251352..56254930hg38UCSC Ensembl
chr4:57117518..57121096hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg383579
hg193579
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18117883
Samples
Known GenesKIAA1211
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6386901
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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