A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362436



Internal ID21019989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:61657170..61661356hg38UCSC Ensembl
chr3:61642844..61647030hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg384187
hg194187
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18101730
Samples
Known GenesPTPRG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362436
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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