A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17534597



Internal ID21858952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:39782554..39782661hg38UCSC Ensembl
chr1:40248226..40248333hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5984122
Supporting Variants
Samples
Known GenesBMP8B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17534597
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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