A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18056897



Internal ID20623938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:2004674..2005630hg38UCSC Ensembl
chr1:1936113..1937069hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg38957
hg19957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6319185
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18056897
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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