A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6551815



Internal ID20924948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:155476280..155476851hg38UCSC Ensembl
chr1:155446071..155446642hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg38572
hg19572
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247117
Samples
Known GenesASH1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6551815
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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