A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362501



Internal ID21020054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:61490065..61504379hg38UCSC Ensembl
chr3:61475739..61490053hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3814315
hg1914315
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4890n223
Supporting Variantsnssv18101711
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362501
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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