A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18056656



Internal ID20623696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:201984187..201987692hg38UCSC Ensembl
chr1:201953315..201956820hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg383506
hg193506
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6322812
Supporting Variants
Samples
Known GenesRNPEP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18056656
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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