A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049602



Internal ID19138821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:78897792..78941161hg38UCSC Ensembl
Innerchr10:80657549..80700918hg19UCSC Ensembl
Innerchr10:80327555..80370924hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3843370
hg1943370
hg1843370
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3512069
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)nsv1049602
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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