A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6413597



Internal ID21071150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:147890779..147898651hg38UCSC Ensembl
chr5:147270342..147278214hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg387873
hg197873
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18126152
Samples
Known GenesC5orf46
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6413597
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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