A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3001359



Internal ID16947625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:36984810..36995509hg38UCSC Ensembl
Outerchr3:37026301..37037000hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg3810700
hg1910700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv954463
Supporting Variants
SamplesBILGI_BIOE
Known GenesEPM2AIP1, MLH1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3001359
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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