A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17616906



Internal ID21808953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:4732420..4732588hg38UCSC Ensembl
chr12:4841586..4841754hg19UCSC Ensembl
Cytoband12p13.32
Allele length
AssemblyAllele length
hg38169
hg19169
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6025216
Supporting Variants
Samples
Known GenesGALNT8
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17616906
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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