A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022871



Internal ID19112089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:60444447..60663649hg38UCSC Ensembl
Innerchr6:57412194..57631396hg19UCSC Ensembl
Innerchr6:57520153..57739355hg18UCSC Ensembl
Cytoband6p11.2
Allele length
AssemblyAllele length
hg38219203
hg19219203
hg18219203
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5970n100
Supporting Variantsnssv3657514
Samples
Known GenesPRIM2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022871
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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