A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6358341



Internal ID21015894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:70498301..70530400hg38UCSC Ensembl
chr3:70547452..70579551hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg3832100
hg1932100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18103699
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6358341
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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