A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006648



Internal ID18749179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16850538..16956580hg38UCSC Ensembl
Innerchr1:17177033..17283075hg19UCSC Ensembl
Innerchr1:17049620..17155662hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38106043
hg19106043
hg18106043
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv107n100
Supporting Variantsnssv3700139, nssv3475506, nssv3463487
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)nsv1006648
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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