A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18005605



Internal ID20572646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:91257862..91258415hg38UCSC Ensembl
chr12:91651639..91652192hg19UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg38554
hg19554
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6475543
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18005605
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00026


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