A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010291



Internal ID18752822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16850538..16934111hg38UCSC Ensembl
Innerchr1:17177033..17260606hg19UCSC Ensembl
Innerchr1:17049620..17133193hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3883574
hg1983574
hg1883574
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv105n100
Supporting Variantsnssv3475372, nssv3466614, nssv3479308, nssv3477247, nssv3476233, nssv3464484, nssv3467788, nssv3465209, nssv3473157, nssv3462928, nssv3468511, nssv3480249, nssv3467959, nssv3700100
Samples
Known GenesCROCC, MIR3675
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1010291
Frequency
Sample Size29084
Observed Gain10
Observed Loss4
Observed Complex0
Frequencyn/a


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