A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5906995



Internal ID22682199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:146888817..146899087hg38UCSC Ensembl
chr6:147209953..147220223hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg3810271
hg1910271
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17412011
Samples
Known GenesSTXBP5-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5906995
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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