A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013701



Internal ID18756233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16855930..16931176hg38UCSC Ensembl
Innerchr1:17182425..17257671hg19UCSC Ensembl
Innerchr1:17055012..17130258hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3875247
hg1975247
hg1875247
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv105n100
Supporting Variantsnssv3481399, nssv3477181, nssv3474750, nssv3475416, nssv3463002, nssv3463766, nssv3700142
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)nsv1013701
Frequency
Sample Size29084
Observed Gain2
Observed Loss5
Observed Complex0
Frequencyn/a


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