A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14336638



Internal ID22283603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:73687954..73688290hg38UCSC Ensembl
chr7:73102284..73102620hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38337
hg19337
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3199075
Supporting Variants
SamplesNA19239
Known GenesWBSCR22
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14336638
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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