A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6318092



Internal ID20851183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151020201..151023900hg38UCSC Ensembl
chr1:150992677..150996376hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg383700
hg193700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053009
Samples
Known GenesPRUNE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6318092
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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