A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014352



Internal ID18756886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16544771..16685003hg38UCSC Ensembl
Innerchr1:16871266..17011498hg19UCSC Ensembl
Innerchr1:16743853..16884085hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38140233
hg19140233
hg18140233
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv50n100
Supporting Variantsnssv3698836
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)nsv1014352
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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