A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6396176



Internal ID21053729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:78972350..78976391hg38UCSC Ensembl
chr5:78268173..78272214hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg384042
hg194042
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18133393
Samples
Known GenesARSB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6396176
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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