A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6414417



Internal ID21071970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:121155238..121435374hg38UCSC Ensembl
chr5:120490933..120771069hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg38280137
hg19280137
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18126526
Samples
Known GenesLOC102467226
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6414417
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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