A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18061058



Internal ID20628098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:35308282..35314491hg38UCSC Ensembl
chr1:35773883..35780092hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg386210
hg196210
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6317144
Supporting Variants
Samples
Known GenesZMYM4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18061058
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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