A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526003



Internal ID20899364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:63713430..64357552hg38UCSC Ensembl
chr18:61380664..62024787hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg38644123
hg19644124
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18043429
Samples
Known GenesHMSD, LINC00305, LOC284294, LOC400654, SERPINB10, SERPINB11, SERPINB2, SERPINB7, SERPINB8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526003
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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