A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6035271



Internal ID21944614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:18234251..18234407hg38UCSC Ensembl
chrUn_gl000212:63003..63159hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38157
hg19157
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17603497
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6035271
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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