A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6323491



Internal ID20856609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:68482934..68484638hg38UCSC Ensembl
chr1:68948617..68950321hg19UCSC Ensembl
Cytoband1p31.2
Allele length
AssemblyAllele length
hg381705
hg191705
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18062730
Samples
Known GenesDEPDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6323491
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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