A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3580109



Internal ID18878390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:105895390..105930798hg38UCSC Ensembl
Innerchr2:106511846..106547254hg19UCSC Ensembl
Innerchr2:105878278..105913686hg18UCSC Ensembl
Cytoband2q12.2
Allele length
AssemblyAllele length
hg3835409
hg1935409
hg1835409
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv999986
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3580109
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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