A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027827



Internal ID18770358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:60389203..60843127hg38UCSC Ensembl
Innerchr6:57361241..57810874hg19UCSC Ensembl
Innerchr6:57469200..57918833hg18UCSC Ensembl
Cytoband6p11.2
Allele length
AssemblyAllele length
hg38453925
hg19449634
hg18449634
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5968n100
Supporting Variantsnssv3745499
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)nsv1027827
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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