A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6139077



Internal ID338261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:586988..670994hg38UCSC Ensembl
chr1:522368..606374hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3884007
hg1984007
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16899351
Samples
Known GenesMIR6723
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6139077
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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