A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012777



Internal ID19101994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:121164999..121256017hg38UCSC Ensembl
Innerchr3:120883846..120974864hg19UCSC Ensembl
Innerchr3:122366536..122457554hg18UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg3891019
hg1991019
hg1891019
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3604526
Samples
Known GenesSTXBP5L
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1012777
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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