A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15192053



Internal ID21330925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:48923506..48923506hg38UCSC Ensembl
chr10:50131551..50131551hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3928975
Supporting Variants
SamplesHG002
Known GenesWDFY4
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15192053
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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