A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6329847



Internal ID20863000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:96457824..96473944hg38UCSC Ensembl
chr1:96923380..96939500hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3816121
hg1916121
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18065335
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6329847
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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