A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012850



Internal ID18755382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:244936197..245533026hg38UCSC Ensembl
Innerchr1:245099499..245696328hg19UCSC Ensembl
Innerchr1:243166122..243762951hg18UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg38596830
hg19596830
hg18596830
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv602n100
Supporting Variantsnssv3493838
Samples
Known GenesEFCAB2, KIF26B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1012850
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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