A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17998396



Internal ID20565436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:23141641..23145634hg38UCSC Ensembl
chr12:23294575..23298568hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg383994
hg193994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6461077
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17998396
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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