A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6315606



Internal ID20848677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151025763..151027017hg38UCSC Ensembl
chr1:150998239..150999493hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg381255
hg191255
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053010
Samples
Known GenesPRUNE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6315606
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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