A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5828180



Internal ID22603115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:161364765..161379331hg38UCSC Ensembl
chr1:161334555..161349121hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3814567
hg1914567
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17461218
Samples
Known GenesC1orf192
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5828180
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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