A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15191091



Internal ID21329949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:37037092..37037092hg38UCSC Ensembl
chr4:37038714..37038714hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3951750
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15191091
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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