A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6330899



Internal ID20864057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:153418883..153419652hg38UCSC Ensembl
chr1:153391359..153392128hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38770
hg19770
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18051977
Samples
Known GenesS100A7A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6330899
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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