A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6318389



Internal ID20851481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:2206701..2222500hg38UCSC Ensembl
chr1:2138140..2153939hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3815800
hg1915800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18058472
Samples
Known GenesC1orf86
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6318389
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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