A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18003603



Internal ID20570643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:75506916..75508273hg38UCSC Ensembl
chr12:75900696..75902053hg19UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg381358
hg191358
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6470354
Supporting Variants
Samples
Known GenesKRR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18003603
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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