A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14329548



Internal ID22136618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:87437826..87438461hg38UCSC Ensembl
chr6:88147544..88148179hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38636
hg19636
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3196476
Supporting Variants
SamplesHG00513
Known GenesC6orf165
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14329548
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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