A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005903



Internal ID18748434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:97206888..97648216hg38UCSC Ensembl
Innerchr2:97872625..98264679hg19UCSC Ensembl
Innerchr2:97236352..97631111hg18UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg38441329
hg19392055
hg18394760
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4025n100
Supporting Variantsnssv3580012
Samples
Known GenesANKRD36, 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)nsv1005903
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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