A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6037582



Internal ID21946925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:13037058..13037122hg38UCSC Ensembl
chr16:13130915..13130979hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17601440
Samples
Known GenesSHISA9
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6037582
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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