A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15191095



Internal ID21329953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:37901687..37901687hg38UCSC Ensembl
chr4:37903308..37903308hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38133
hg19133
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3928933
Supporting Variants
SamplesHG002
Known GenesTBC1D1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15191095
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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