A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14296607



Internal ID22117345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:161074741..161075231hg38UCSC Ensembl
chr2:161931252..161931742hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg38491
hg19491
Variant TypeOTHER sequence alteration
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3557643
Supporting Variants
SamplesHG00512
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14296607
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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