A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18133787



Internal ID20700827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:91388131..91392989hg38UCSC Ensembl
chr5:90683948..90688806hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg384859
hg194859
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6404881
Supporting Variants
Samples
Known GenesARRDC3-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18133787
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00018


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