A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6328344



Internal ID20861491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:241992942..242005036hg38UCSC Ensembl
chr1:242156244..242168338hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg3812095
hg1912095
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18059114
Samples
Known GenesMAP1LC3C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6328344
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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