A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063350



Internal ID19152569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:7215277..7660001hg38UCSC Ensembl
Innerchr18:7215275..7659999hg19UCSC Ensembl
Innerchr18:7205275..7649999hg18UCSC Ensembl
Cytoband18p11.23
Allele length
AssemblyAllele length
hg38444725
hg19444725
hg18444725
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3725281
Samples
Known GenesLRRC30, PTPRM
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063350
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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