A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18000725



Internal ID20567765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:31976265..31980075hg38UCSC Ensembl
chr12:32129199..32133009hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg383811
hg193811
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6456181
Supporting Variants
Samples
Known GenesKIAA1551
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18000725
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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