A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053577



Internal ID19142796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:15884287..15906234hg38UCSC Ensembl
Innerchr10:15926286..15948233hg19UCSC Ensembl
Innerchr10:15966292..15988239hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3821948
hg1921948
hg1821948
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv681n100
Supporting Variantsnssv3522639
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)nsv1053577
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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