A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18133786



Internal ID20700826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:91383201..91383700hg38UCSC Ensembl
chr5:90679018..90679517hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6402465
Supporting Variants
Samples
Known GenesARRDC3, ARRDC3-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18133786
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00982


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