A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18001432



Internal ID20568472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:5311745..5325046hg38UCSC Ensembl
chr12:5420911..5434212hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg3813302
hg1913302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6472181
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18001432
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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