A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014177



Internal ID19103397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:146089972..146109354hg38UCSC Ensembl
Innerchr2:146847540..146866922hg19UCSC Ensembl
Innerchr2:146564010..146583392hg18UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg3819383
hg1919383
hg1819383
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4088n100
Supporting Variantsnssv3582836, nssv3582831, nssv3582830, nssv3582828, nssv3582835, nssv3582840, nssv3582838, nssv3582837, nssv3582841, nssv3582834, nssv3729248, nssv3582832, nssv3582842, nssv3582839, nssv3582833, nssv3582829
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1014177
Frequency
Sample Size11257
Observed Gain16
Observed Loss0
Observed Complex0
Frequencyn/a


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