A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18045942



Internal ID20612982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:14488763..14490911hg38UCSC Ensembl
chr19:14599575..14601723hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg382149
hg192149
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6518971
Supporting Variants
Samples
Known GenesGIPC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18045942
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00049


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