A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18051297



Internal ID20618337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:12028701..12032600hg38UCSC Ensembl
chr1:12088758..12092657hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg383900
hg193900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6316186
Supporting Variants
Samples
Known GenesMIIP, MIR6729
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18051297
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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