A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5827595



Internal ID22602525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:109129317..109140982hg38UCSC Ensembl
chr1:109671939..109683604hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3811666
hg1911666
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17456734
Samples
Known GenesKIAA1324
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5827595
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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