A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6330702



Internal ID20863860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:106222343..106291984hg38UCSC Ensembl
chr1:106764965..106834606hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3869642
hg1969642
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18051578
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6330702
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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