A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3791n100



Internal ID20155407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:39914636..40018324hg38UCSC Ensembl
chr2:40141776..40245464hg19UCSC Ensembl
chr2:39995280..40098968hg18UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg38103689
hg19103689
hg18103689
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1003920, nsv1000423
Samples
Known GenesSLC8A1-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3791n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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