A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6320384



Internal ID20853482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:94956758..94965761hg38UCSC Ensembl
chr1:95422314..95431317hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg389004
hg199004
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18066079
Samples
Known GenesLOC729970
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6320384
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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