A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5461484



Internal ID239433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:10922237..10922288hg38UCSC Ensembl
chr6:10922470..10922521hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16978984
Samples
Known GenesSYCP2L
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5461484
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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