A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6147197



Internal ID346379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6590207..6590207hg38UCSC Ensembl
chr10:6632169..6632169hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg381
hg191
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17029002
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6147197
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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