A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568230



Internal ID16008953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22777657..23119335hg38UCSC Ensembl
Innerchr15:22753733..23095411hg19UCSC Ensembl
Innerchr15:20305097..20646852hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38341679
hg19341679
hg18341756
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4317n54
Supporting Variantsnssv838344, nssv838343
Samples
Known GenesCYFIP1, LOC283683, NIPA1, NIPA2, TUBGCP5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568230
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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