A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6412962



Internal ID21070515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:76487162..76619580hg38UCSC Ensembl
chr5:75782987..75915405hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg38132419
hg19132419
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216586
Samples
Known GenesF2RL2, IQGAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6412962
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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