A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6321695



Internal ID20854803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:86896901..86925400hg38UCSC Ensembl
chr1:87362584..87391083hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg3828500
hg1928500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205189
Samples
Known GenesHS2ST1, SEP15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6321695
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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