A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3957367



Internal ID19220457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:68266952..68267009hg38UCSC Ensembl
Outerchr3:68316102..68316159hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1127965
Supporting Variants
SamplesKWS1
Known GenesFAM19A1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3957367
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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