A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6317772



Internal ID20850861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:104399701..104487400hg38UCSC Ensembl
chr1:104942323..105030022hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3887700
hg1987700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18050312
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6317772
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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