A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6369930



Internal ID21027483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:61873956..61874932hg38UCSC Ensembl
chr3:61859630..61860606hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38977
hg19977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18101752
Samples
Known GenesPTPRG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6369930
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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