A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15185900



Internal ID21324712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:58863528..58863528hg38UCSC Ensembl
chr18:56530760..56530760hg19UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg38157
hg19157
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3938315
Supporting Variants
SamplesHG002
Known GenesZNF532
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15185900
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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