A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4015n100



Internal ID22790102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:97065384..97545714hg38UCSC Ensembl
chr2:97731121..98162177hg19UCSC Ensembl
chr2:97094848..97528609hg18UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg38480331
hg19431057
hg18433762
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1003980, nsv1013849, nsv1013489
Samples
Known GenesANKRD36, ANKRD36B, FAHD2B, LOC100506076, LOC100506123
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4015n100
Frequency
Sample Size11257
Observed Gain7
Observed Loss11
Observed Complex0
Frequencyn/a


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