A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6414247



Internal ID21071800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:77689087..77690406hg38UCSC Ensembl
chr5:76984912..76986231hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg381320
hg191320
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18135136
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6414247
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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