A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3952028



Internal ID21372097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:27743756..27744104hg38UCSC Ensembl
chr7:27783375..27783723hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg38349
hg19349
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15198538
SamplesHG002
Known GenesTAX1BP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3952028
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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