A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17455728



Internal ID22513605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:155546981..155548985hg38UCSC Ensembl
chr1:155516772..155518776hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg382005
hg192005
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5828363
Supporting Variants
Samples
Known GenesASH1L
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17455728
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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