A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6031857



Internal ID21941200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:2999723..3000703hg38UCSC Ensembl
chr18:2999721..3000701hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg38981
hg19981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17621337
Samples
Known GenesLPIN2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6031857
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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