A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6328115



Internal ID20861260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:167741364..167746462hg38UCSC Ensembl
chr1:167710601..167715699hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg385099
hg195099
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053569
Samples
Known GenesMPZL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6328115
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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