A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006877



Internal ID18749408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:15642115..15707706hg38UCSC Ensembl
Innerchr1:15968610..16034201hg19UCSC Ensembl
Innerchr1:15841197..15906788hg18UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3865592
hg1965592
hg1865592
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3698786
Samples
Known GenesDDI2, PLEKHM2, RSC1A1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1006877
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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