A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6412261



Internal ID21069814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:81140104..81189611hg38UCSC Ensembl
chr5:80435923..80485430hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg3849508
hg1949508
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18134140
Samples
Known GenesRASGRF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6412261
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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