A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17455267



Internal ID22513144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:15188630..15223921hg38UCSC Ensembl
chr1:15515126..15550417hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3835292
hg1935292
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5828234
Supporting Variants
Samples
Known GenesTMEM51
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17455267
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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