A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6036743



Internal ID21946086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:12208068..12226174hg38UCSC Ensembl
chr18:12208067..12226173hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3818107
hg1918107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17633365
Samples
Known GenesC18orf61
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6036743
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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