A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18050957



Internal ID20617997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:112607501..112609400hg38UCSC Ensembl
chr1:113150123..113152022hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6317205
Supporting Variants
Samples
Known GenesST7L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18050957
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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