A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6377062



Internal ID21034615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:37698219..37698880hg38UCSC Ensembl
chr5:37698321..37698982hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg38662
hg19662
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18132036
Samples
Known GenesWDR70
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6377062
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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