A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4010n100



Internal ID22790097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:97043967..97608974hg38UCSC Ensembl
chr2:97709704..98225437hg19UCSC Ensembl
chr2:97073431..97591869hg18UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg38565008
hg19515734
hg18518439
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1004229, nsv1009571, nsv999329, nsv1009372, nsv1004521, nsv1003620
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)dgv4010n100
Frequency
Sample Size11257
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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