A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5896231



Internal ID22671320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:150605624..150611831hg38UCSC Ensembl
chr6:150926760..150932967hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg386208
hg196208
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17427114
Samples
Known GenesPLEKHG1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5896231
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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