A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17635725



Internal ID21827772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:42581943..42945188hg38UCSC Ensembl
chr19:43086095..43449340hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38363246
hg19363246
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6045530
Supporting Variants
Samples
Known GenesCEACAM8, LIPE-AS1, LOC100289650, PSG1, PSG10P, PSG3, PSG6, PSG7, PSG8
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17635725
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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