A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6404118



Internal ID21061671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:111509964..111523519hg38UCSC Ensembl
chr5:110845662..110859217hg19UCSC Ensembl
Cytoband5q22.1
Allele length
AssemblyAllele length
hg3813556
hg1913556
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18124992
Samples
Known GenesSTARD4, STARD4-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6404118
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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