A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15196541



Internal ID21335337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:154634583..154634638hg38UCSC Ensembl
chr4:155555735..155555790hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3939800
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15196541
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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