A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6035139



Internal ID21944482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:21592346..21592525hg38UCSC Ensembl
chr18:19172307..19172486hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38180
hg19180
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17618780
Samples
Known GenesESCO1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6035139
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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