A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6394957



Internal ID21052510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:28830105..28830670hg38UCSC Ensembl
chr5:28830212..28830777hg19UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg38566
hg19566
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18128895
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6394957
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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