A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3004463



Internal ID16950729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:178832325..178833073hg38UCSC Ensembl
Outerchr3:178550113..178550861hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg38749
hg19749
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv955526
Supporting Variants
SamplesBILGI_BIOE
Known GenesKCNMB2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3004463
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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