A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012476



Internal ID19101693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:65459064..65484195hg38UCSC Ensembl
Innerchr1:65924747..65949878hg19UCSC Ensembl
Innerchr1:65697335..65722466hg18UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3825132
hg1925132
hg1825132
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3701248
Samples
Known GenesLEPR
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1012476
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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