A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17451245



Internal ID22509117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:124210945..124212294hg38UCSC Ensembl
chr12:124695491..124696840hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg381350
hg191350
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5849080
Supporting Variants
Samples
Known GenesZNF664-FAM101A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17451245
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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