A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14332688



Internal ID22116960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:38452201..38454003hg38UCSC Ensembl
chr7:38491801..38493603hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg381803
hg191803
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3190788
Supporting Variants
SamplesHG00512
Known GenesAMPH
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14332688
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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