A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3957398



Internal ID18875448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:122934025..122935811hg38UCSC Ensembl
Outerchr3:122652872..122654658hg19UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg381787
hg191787
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1127989
Supporting Variants
SamplesKWS1
Known GenesSEMA5B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3957398
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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