A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049693



Internal ID19138912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:126881026..126925770hg38UCSC Ensembl
Innerchr10:128569595..128614339hg19UCSC Ensembl
Innerchr10:128559585..128604329hg18UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3844745
hg1944745
hg1844745
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3706256
Samples
Known GenesDOCK1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1049693
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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