A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6363305



Internal ID21020858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:77058153..77064787hg38UCSC Ensembl
chr3:77107304..77113938hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg386635
hg196635
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18105132
Samples
Known GenesROBO2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6363305
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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