A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17465900



Internal ID22523790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:124240927..124242226hg38UCSC Ensembl
chr12:124725473..124726772hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5863509
Supporting Variants
Samples
Known GenesZNF664-FAM101A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17465900
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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