A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6333708



Internal ID20866888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:8853320..8855037hg38UCSC Ensembl
chr1:8913379..8915096hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg381718
hg191718
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18064607
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6333708
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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