A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2996567



Internal ID16942833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:185065413..185078212hg38UCSC Ensembl
Outerchr3:184783201..184796000hg19UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg3812800
hg1912800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv950020
Supporting Variants
SamplesBILGI_BIOE
Known GenesC3orf70
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2996567
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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