A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17997566



Internal ID20564606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:12879339..12905014hg38UCSC Ensembl
chr12:13032273..13057948hg19UCSC Ensembl
Cytoband12p13.1
Allele length
AssemblyAllele length
hg3825676
hg1925676
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6465621
Supporting Variants
Samples
Known GenesGPRC5A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17997566
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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