A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6319500



Internal ID20852595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:155446553..155449188hg38UCSC Ensembl
chr1:155416344..155418979hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg382636
hg192636
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052075
Samples
Known GenesASH1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6319500
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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