A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6390334



Internal ID21047887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:55560737..55561023hg38UCSC Ensembl
chr4:56426904..56427190hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38287
hg19287
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18118371
Samples
Known GenesPDCL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6390334
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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