A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17995629



Internal ID20562669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:10319017..10329391hg38UCSC Ensembl
chr12:10471616..10481990hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg3810375
hg1910375
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6456997
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17995629
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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