A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15198538



Internal ID21337334
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 StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3952028
Supporting Variants
SamplesHG002
Known GenesTAX1BP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15198538
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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