A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011759



Internal ID18754293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16544771..16685915hg38UCSC Ensembl
Innerchr1:16871266..17012410hg19UCSC Ensembl
Innerchr1:16743853..16884997hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38141145
hg19141145
hg18141145
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv50n100
Supporting Variantsnssv3698837
Samples
Known GenesCROCCP2, LOC729574, MIR3675, MST1P2, NBPF1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1011759
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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