A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17361579



Internal ID22587248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:93803646..93808913hg38UCSC Ensembl
chr12:94197422..94202689hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg385268
hg195268
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5939383
Supporting Variants
Samples
Known GenesCRADD
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17361579
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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