A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3191355



Internal ID22342071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:39753551..39753631hg38UCSC Ensembl
chr7:39793150..39793230hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14332772
SamplesHG00732
Known GenesLINC00265
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3191355
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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