A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568913



Internal ID16356322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32633875..33060788hg38UCSC Ensembl
Innerchr15:32926076..33352989hg19UCSC Ensembl
Innerchr15:30713368..31140281hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38426914
hg19426914
hg18426914
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149582
SamplesNINDS_129
Known GenesARHGAP11A, FMN1, GREM1, LOC100131315, SCG5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568913
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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