A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17480388



Internal ID22538291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:7165555..7208306hg38UCSC Ensembl
chr19:7165566..7208317hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3842752
hg1942752
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5871451
Supporting Variants
Samples
Known GenesINSR
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17480388
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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