A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010167



Internal ID19099386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:97360488..97657156hg38UCSC Ensembl
Innerchr2:98013814..98273619hg19UCSC Ensembl
Innerchr2:97379953..97640051hg18UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg38296669
hg19259806
hg18260099
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4026n100
Supporting Variantsnssv3580037
Samples
Known GenesACTR1B, ANKRD36B, COX5B, 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)nsv1010167
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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