A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3001471



Internal ID16947737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:137759259..137771558hg38UCSC Ensembl
Outerchr3:137478101..137490400hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg3812300
hg1912300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv955354
Supporting Variants
SamplesBILGI_BIOE
Known GenesSOX14
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3001471
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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