A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6411560



Internal ID21069113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:72249008..72253882hg38UCSC Ensembl
chr5:71544835..71549709hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg384875
hg194875
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18132149
Samples
Known GenesMRPS27
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6411560
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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