A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15176750



Internal ID21315546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:50906590..50906657hg38UCSC Ensembl
chr19:51409846..51409913hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3945366
Supporting Variants
SamplesHG002
Known GenesKLK4
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15176750
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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