A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3997733



Internal ID18845399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:149760954..149790529hg38UCSC Ensembl
Outerchr6:150082090..150111665hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3829576
hg1929576
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1148946
Supporting Variants
SamplesKWB1
Known GenesPCMT1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3997733
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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