A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044700



Internal ID18787231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:87855368..87881536hg38UCSC Ensembl
Innerchr10:89615125..89641293hg19UCSC Ensembl
Innerchr10:89605105..89631273hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3826169
hg1926169
hg1826169
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3516363
Samples
Known GenesKLLN, PTEN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044700
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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