A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3579481



Internal ID18877762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:91460974..91751200hg38UCSC Ensembl
Innerchr2:91653350..91939226hg19UCSC Ensembl
Innerchr2:91017077..91302953hg18UCSC Ensembl
Cytoband2p11.1
Allele length
AssemblyAllele length
hg38290227
hg19285877
hg18285877
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1010194
Supporting Variants
Samples
Known GenesLOC654342
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3579481
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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