A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6396184



Internal ID21053737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:72587533..72589807hg38UCSC Ensembl
chr5:71883360..71885634hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg382275
hg192275
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18132160
Samples
Known GenesLOC102477328
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6396184
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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