A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007618



Internal ID18750149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16544771..16643493hg38UCSC Ensembl
Innerchr1:16871266..16969988hg19UCSC Ensembl
Innerchr1:16743853..16842575hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3898723
hg1998723
hg1898723
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv46n100
Supporting Variantsnssv3475836
Samples
Known GenesCROCCP2, MIR3675, NBPF1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1007618
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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