A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368250



Internal ID21025803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:73570511..73570961hg38UCSC Ensembl
chr3:73619662..73620112hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38451
hg19451
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18103844
Samples
Known GenesPDZRN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368250
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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