A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327951



Internal ID20861095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:46672666..46673047hg38UCSC Ensembl
chr1:47138338..47138719hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg38382
hg19382
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18061576
Samples
Known GenesTEX38
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327951
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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