A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14338775



Internal ID22281998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155812901..155816200hg38UCSC Ensembl
chr7:155605595..155608894hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg383300
hg193300
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3225333
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14338775
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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