A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16273205



Internal ID20482423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:180272087..180272087hg38UCSC Ensembl
chr1:180241222..180241222hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4764612
Supporting Variants
Samples
Known GenesLHX4, LOC100527964
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16273205
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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