A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004702



Internal ID19093919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:21651394..21711459hg38UCSC Ensembl
Innerchr2:21874266..21934331hg19UCSC Ensembl
Innerchr2:21727771..21787836hg18UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg3860066
hg1960066
hg1860066
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3579010
Samples
Known GenesLOC645949
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1004702
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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