A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3989235



Internal ID18892503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:154125780..154126102hg38UCSC Ensembl
Outerchr6:154446915..154447237hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1135663
Supporting Variants
SamplesKWS2
Known GenesOPRM1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3989235
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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