A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16264910



Internal ID20474128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:155547037..155547210hg38UCSC Ensembl
chr1:155516828..155517001hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg38174
hg19174
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4734214
Supporting Variants
Samples
Known GenesASH1L
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16264910
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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