A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3579546



Internal ID18877827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:95504810..95712480hg38UCSC Ensembl
Innerchr2:96170558..96378228hg19UCSC Ensembl
Innerchr2:95534285..95741955hg18UCSC Ensembl
Cytoband2q11.1
Allele length
AssemblyAllele length
hg38207671
hg19207671
hg18207671
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv998587
Supporting Variants
Samples
Known GenesTRIM43
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3579546
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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