A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15200729



Internal ID21339525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:43947984..43947984hg38UCSC Ensembl
chr4:43950001..43950001hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3934358
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15200729
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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