A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3994135



Internal ID18867755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:166162740..166162827hg38UCSC Ensembl
Outerchr6:166576228..166576315hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1142648
Supporting Variants
SamplesKWS1
Known GenesT
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3994135
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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