A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6322707



Internal ID20855821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:103456109..103456569hg38UCSC Ensembl
chr1:103998731..103999191hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg38461
hg19461
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18050215
Samples
Known GenesLOC101928436
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6322707
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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