A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15197964



Internal ID21336760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:170191552..170191818hg38UCSC Ensembl
chr6:170506776..170507042hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38267
hg19267
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3949425
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15197964
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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