A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6406075



Internal ID21063628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:72082740..72087354hg38UCSC Ensembl
chr5:71378567..71383181hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg384615
hg194615
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18132142
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6406075
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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