A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6365571



Internal ID21023124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:751877..1558879hg38UCSC Ensembl
chr3:793560..1600563hg19UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38807003
hg19807004
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18102322
Samples
Known GenesCNTN6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6365571
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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