A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001568



Internal ID19090785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:34466002..34512477hg38UCSC Ensembl
Innerchr2:34691069..34737544hg19UCSC Ensembl
Innerchr2:34544573..34591048hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg3846476
hg1946476
hg1846476
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3761n100
Supporting Variantsnssv3728117, nssv3575205
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)nsv1001568
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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