A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17370091



Internal ID22595760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:60604039..60604349hg38UCSC Ensembl
chr1:61069711..61070021hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5880951
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17370091
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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