A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6384997



Internal ID21042550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:135912412..135913135hg38UCSC Ensembl
chr4:136833567..136834290hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38724
hg19724
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18107288
Samples
Known GenesLINC00613
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6384997
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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