A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6356227



Internal ID21013780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:61492598..61507135hg38UCSC Ensembl
chr3:61478272..61492809hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3814538
hg1914538
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4890n223
Supporting Variantsnssv18101713
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6356227
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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