A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013177



Internal ID19102395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:33889..206851hg38UCSC Ensembl
Innerchr2:33889..206851hg19UCSC Ensembl
Innerchr2:23889..196851hg18UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg38172963
hg19172963
hg18172963
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3726654
Samples
Known GenesFAM110C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013177
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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