A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17079206



Internal ID21445235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:3095499..3095627hg38UCSC Ensembl
chr12:3204665..3204793hg19UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg38129
hg19129
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5590243
Supporting Variants
SamplesHG00732
Known GenesTSPAN9
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17079206
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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