A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14338575



Internal ID22205971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149585155..149608808hg38UCSC Ensembl
chr7:149282246..149305899hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3823654
hg1923654
Variant TypeCNV duplication
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3222612
Supporting Variants
SamplesHG00732
Known GenesZNF767
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14338575
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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