A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545670



Internal ID15986393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16856620..16941001hg38UCSC Ensembl
Innerchr1:17183115..17267496hg19UCSC Ensembl
Innerchr1:17055702..17140083hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3884382
hg1984382
hg1884382
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv166n54
Supporting Variantsnssv710893, nssv710890, nssv710894, nssv710891, nssv710892, nssv710889
Samples
Known GenesCROCC, MIR3675
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545670
Frequency
Sample Size17421
Observed Gain2
Observed Loss4
Observed Complex0
Frequencyn/a


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