A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17463857



Internal ID22521743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:45385820..45389589hg38UCSC Ensembl
chr12:45779603..45783372hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg383770
hg193770
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5850171
Supporting Variants
Samples
Known GenesANO6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17463857
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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