A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6392970



Internal ID21050523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:37075673..37076128hg38UCSC Ensembl
chr5:37075775..37076230hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg38456
hg19456
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18131999
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6392970
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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