A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6330947



Internal ID20864106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23474154..23477099hg38UCSC Ensembl
chr1:23800647..23803592hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg382946
hg192946
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18058821
Samples
Known GenesASAP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6330947
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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