A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17535604



Internal ID21859959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:37440487..37452484hg38UCSC Ensembl
chr1:37906088..37918085hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3811998
hg1911998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5984077
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17535604
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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