A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5886796



Internal ID22661785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:109129240..109178694hg38UCSC Ensembl
chr1:109671862..109721316hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3849455
hg1949455
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17359621
Samples
Known GenesKIAA1324
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5886796
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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