A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6315997



Internal ID20849073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:214883005..214883595hg38UCSC Ensembl
chr1:215056348..215056938hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38591
hg19591
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18057827
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6315997
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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