A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5562244



Internal ID335202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:87566926..87568013hg38UCSC Ensembl
chr6:88276644..88277731hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg381088
hg191088
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16985000
Samples
Known GenesRARS2
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5562244
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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