A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6388818



Internal ID21046371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:136514201..136556800hg38UCSC Ensembl
chr4:137435356..137477955hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3842600
hg1942600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18107383
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6388818
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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