A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012812



Internal ID18755344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16888315..16949734hg38UCSC Ensembl
Innerchr1:17214810..17276229hg19UCSC Ensembl
Innerchr1:17087397..17148816hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3861420
hg1961420
hg1861420
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv116n100
Supporting Variantsnssv3476752, nssv3700269, nssv3478009, nssv3480398, nssv3469895, nssv3473902, nssv3479672, nssv3470732, nssv3700268
Samples
Known GenesCROCC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1012812
Frequency
Sample Size29084
Observed Gain7
Observed Loss2
Observed Complex0
Frequencyn/a


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