A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3529142



Internal ID22398535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:124076763..124076842hg38UCSC Ensembl
chr7:123716817..123716896hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14337390
SamplesHG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3529142
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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