A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18049645



Internal ID20616685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:101065084..101077591hg38UCSC Ensembl
chr1:101530640..101543147hg19UCSC Ensembl
Cytoband1p21.2
Allele length
AssemblyAllele length
hg3812508
hg1912508
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6321746
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18049645
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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