A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17367957



Internal ID22593626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:101501480..101501551hg38UCSC Ensembl
chr12:101895258..101895329hg19UCSC Ensembl
Cytoband12q23.2
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5942333
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17367957
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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