A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6328915



Internal ID20862065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:156046303..156047623hg38UCSC Ensembl
chr1:156016094..156017414hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg381321
hg191321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052250
Samples
Known GenesMIR7851, UBQLN4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6328915
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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