A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17355421



Internal ID22581090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:155388956..155389244hg38UCSC Ensembl
chr1:155358747..155359035hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg38289
hg19289
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5873930
Supporting Variants
Samples
Known GenesASH1L
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17355421
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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