A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327354



Internal ID20860492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:7931122..7938757hg38UCSC Ensembl
chr1:7991182..7998817hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg387636
hg197636
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18064270
Samples
Known GenesTNFRSF9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327354
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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