A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3975159



Internal ID18888359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:138103249..138103317hg38UCSC Ensembl
Outerchr6:138424386..138424454hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1140702
Supporting Variants
SamplesKWS2
Known GenesPERP
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3975159
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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