A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6318121



Internal ID20851212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:219168079..219177172hg38UCSC Ensembl
chr1:219341421..219350514hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg389094
hg199094
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18058118
Samples
Known GenesLOC643723, LYPLAL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6318121
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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