A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6414442



Internal ID21071995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:61964362..61972033hg38UCSC Ensembl
chr5:61260189..61267860hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg387672
hg197672
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18131846
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6414442
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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