A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3529255



Internal ID22398648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:96133879..96134101hg38UCSC Ensembl
chr7:95763191..95763413hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38223
hg19223
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14335476, nssv14335477, nssv14335478, nssv14335474, nssv14335475, nssv14335472, nssv14335473
SamplesHG00512, NA19238, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesSLC25A13
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3529255
Frequency
Sample Size9
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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