A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008038



Internal ID18750569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16850538..16932813hg38UCSC Ensembl
Innerchr1:17177033..17259308hg19UCSC Ensembl
Innerchr1:17049620..17131895hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3882276
hg1982276
hg1882276
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv105n100
Supporting Variantsnssv3468151, nssv3471209, nssv3479928, nssv3479271, nssv3470753, nssv3471768, nssv3467536, nssv3464629, nssv3478898, nssv3468304, nssv3474510, nssv3469751, nssv3473241, nssv3470960, nssv3482226, nssv3480821, nssv3700099, nssv3478963, nssv3475863, nssv3476971, nssv3475890, nssv3472117, nssv3468547, nssv3469225, nssv3473869, nssv3478087
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)nsv1008038
Frequency
Sample Size29084
Observed Gain24
Observed Loss2
Observed Complex0
Frequencyn/a


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