A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6318519



Internal ID20851611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:209387485..209388306hg38UCSC Ensembl
chr1:209560830..209561651hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg38822
hg19822
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18057250
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6318519
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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