A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3995n100



Internal ID22790082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:91460974..91602710hg38UCSC Ensembl
chr2:91653350..91790736hg19UCSC Ensembl
chr2:91017077..91154463hg18UCSC Ensembl
Cytoband2p11.1
Allele length
AssemblyAllele length
hg38141737
hg19137387
hg18137387
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv999855, nsv1004862
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3995n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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