A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6319991



Internal ID20853089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:91643518..91644075hg38UCSC Ensembl
chr1:92109075..92109632hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg38558
hg19558
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18065145
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6319991
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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