A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6415197



Internal ID21072750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:126180501..126182300hg38UCSC Ensembl
chr5:125516194..125517993hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18123712
Samples
Known GenesLOC102546228
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6415197
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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