A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14337062



Internal ID22219620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:141747383..141748018hg38UCSC Ensembl
chr7:141447183..141447818hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38636
hg19636
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3229329
Supporting Variants
SamplesHG00733
Known GenesSSBP1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14337062
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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