A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022933



Internal ID18765467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:57444185..60783732hg38UCSC Ensembl
Innerchr6:57308983..57751479hg19UCSC Ensembl
Innerchr6:57416942..57859438hg18UCSC Ensembl
Cytoband6p11.2
Allele length
AssemblyAllele length
hg383339548
hg19442497
hg18442497
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5968n100
Supporting Variantsnssv3745496
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)nsv1022933
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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