A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014277



Internal ID19103498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:99158818..99234905hg38UCSC Ensembl
Innerchr3:98877662..98953749hg19UCSC Ensembl
Innerchr3:100360352..100436439hg18UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg3876088
hg1976088
hg1876088
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4821n100
Supporting Variantsnssv3603333
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)nsv1014277
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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