A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6139773



Internal ID338962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:236038701..236038862hg38UCSC Ensembl
chr1:236202001..236202162hg19UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg38162
hg19162
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16898406
Samples
Known GenesNID1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6139773
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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