A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6316047



Internal ID20849123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:93885000..93891113hg38UCSC Ensembl
chr1:94350556..94356669hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg386114
hg196114
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18065591
Samples
Known GenesGCLM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6316047
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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