A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6330541



Internal ID20863698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:162071222..162075031hg38UCSC Ensembl
chr1:162041012..162044821hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg383810
hg193810
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053300
Samples
Known GenesNOS1AP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6330541
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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