A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17450335



Internal ID22508205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:3900717..3909641hg38UCSC Ensembl
chr1:3817281..3826205hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg388925
hg198925
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5830192
Supporting Variants
Samples
Known GenesLINC01134
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17450335
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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