A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3557643



Internal ID22426448
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14296609, nssv14296611, nssv14296610, nssv14296607, nssv14296608
SamplesHG00512, HG00732, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3557643
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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