A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4181n100



Internal ID22790268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:231055301..231131114hg38UCSC Ensembl
chr2:231920015..231995828hg19UCSC Ensembl
chr2:231628259..231704072hg18UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg3875814
hg1975814
hg1875814
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1013780, nsv1005656
Samples
Known GenesHTR2B, PSMD1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4181n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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