A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18101730



Internal ID20668770
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 StatusS
Merged Variantsnsv6362436
Supporting Variants
Samples
Known GenesPTPRG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18101730
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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