A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17352594



Internal ID22578263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:51304774..51305093hg38UCSC Ensembl
chr12:51698558..51698877hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5939504
Supporting Variants
Samples
Known GenesBIN2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17352594
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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