A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15191248



Internal ID21330109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:86469249..86469249hg38UCSC Ensembl
chr10:88229006..88229006hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3943733
Supporting Variants
SamplesHG002
Known GenesWAPAL
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15191248
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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