A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6319697



Internal ID20852792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:73972501..74189300hg38UCSC Ensembl
chr1:74438184..74654984hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38216800
hg19216801
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204398
Samples
Known GenesLRRIQ3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6319697
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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