A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5461220



Internal ID239181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:11555173..11560104hg38UCSC Ensembl
chr6:11555406..11560337hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg384932
hg194932
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16980983
Samples
Known GenesTMEM170B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5461220
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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