A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15203989



Internal ID21342795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:132698175..132698175hg38UCSC Ensembl
chr7:132382934..132382934hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3950061
Supporting Variants
SamplesHG002
Known GenesFLJ40288
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15203989
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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