A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14329217



Internal ID22261324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:69749843..69750083hg38UCSC Ensembl
chr6:70459735..70459975hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38241
hg19241
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3529567
Supporting Variants
SamplesNA19238
Known GenesLMBRD1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14329217
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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