A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6397164



Internal ID21054717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:87308601..87309800hg38UCSC Ensembl
chr5:86604418..86605617hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18136118
Samples
Known GenesRASA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6397164
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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