A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6140631



Internal ID339824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149564790..149571000hg38UCSC Ensembl
chr6:149885926..149892136hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg386211
hg196211
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16988993
Samples
Known GenesGINM1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6140631
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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