A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545688



Internal ID15986411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16921023..16935243hg38UCSC Ensembl
Innerchr1:17247518..17261738hg19UCSC Ensembl
Innerchr1:17120105..17134325hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3814221
hg1914221
hg1814221
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv171n54
Supporting Variantsnssv710919, nssv710921, nssv710920
Samples
Known GenesCROCC
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545688
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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