A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17610336



Internal ID21802383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:56559595..56559757hg38UCSC Ensembl
chr12:56953379..56953541hg19UCSC Ensembl
Cytoband12q13.3
Allele length
AssemblyAllele length
hg38163
hg19163
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6035272
Supporting Variants
Samples
Known GenesRBMS2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17610336
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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