A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17481069



Internal ID22538973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:58102328..58116038hg38UCSC Ensembl
chr1:58568000..58581710hg19UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg3813711
hg1913711
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5830406
Supporting Variants
Samples
Known GenesDAB1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17481069
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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