A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3527633



Internal ID22397020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:98049529..98049678hg38UCSC Ensembl
chr7:97678841..97678990hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14335547, nssv14335542, nssv14335540, nssv14335546, nssv14335548, nssv14335541, nssv14335544, nssv14335545, nssv14335543
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3527633
Frequency
Sample Size9
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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