A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051555



Internal ID18794086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:132295188..132415461hg38UCSC Ensembl
Innerchr10:134108692..134228965hg19UCSC Ensembl
Innerchr10:133958682..134078955hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38120274
hg19120274
hg18120274
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3520485
Samples
Known GenesLRRC27, PWWP2B, STK32C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051555
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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