A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18197788



Internal ID20764828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35818262..36019433hg38UCSC Ensembl
chr19:36309164..36510335hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38201172
hg19201172
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6532655
Supporting Variants
Samples
Known GenesALKBH6, APLP1, CLIP3, HCST, KIRREL2, LRFN3, NFKBID, NPHS1, SDHAF1, SYNE4, TYROBP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18197788
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00046


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