A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17352932



Internal ID22578601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:97275425..97275488hg38UCSC Ensembl
chr12:97669203..97669266hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5937503
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17352932
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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