A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3220528



Internal ID22365197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:157048084..157048192hg38UCSC Ensembl
chr7:156840778..156840886hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14338863
SamplesHG00512
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3220528
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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