A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18065095



Internal ID20632135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:90922237..90922628hg38UCSC Ensembl
chr1:91387794..91388185hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg38392
hg19392
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6316343
Supporting Variants
Samples
Known GenesZNF644
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18065095
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00051


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