A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3932626



Internal ID21352695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:95986358..95986358hg38UCSC Ensembl
chr10:97746115..97746115hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg38248
hg19248
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15191675
SamplesHG002
Known GenesENTPD1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3932626
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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