A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18134412



Internal ID20701452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:75079125..75089586hg38UCSC Ensembl
chr5:74374950..74385411hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg3810462
hg1910462
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6397349
Supporting Variants
Samples
Known GenesANKRD31
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18134412
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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