A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17464898



Internal ID22522786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:37938614..37947371hg38UCSC Ensembl
chr1:38404286..38413043hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg388758
hg198758
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5830004
Supporting Variants
Samples
Known GenesINPP5B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17464898
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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