A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3210085



Internal ID22358060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:75048266..75058095hg38UCSC Ensembl
chr7:74462375..74472202hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg389830
hg199828
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8602n152
Supporting Variantsnssv14337327
SamplesNA19240
Known GenesWBSCR16
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3210085
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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