A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6316016



Internal ID20849092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25214023..25215071hg38UCSC Ensembl
chr1:25540514..25541562hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg381049
hg191049
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060289
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6316016
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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