A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6377739



Internal ID21035292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:103405848..103406440hg38UCSC Ensembl
chr4:104327005..104327597hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38593
hg19593
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18107572
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6377739
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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