A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615936



Internal ID16403345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135906813..135907886hg38UCSC Ensembl
Innerchr9:138798659..138799732hg19UCSC Ensembl
Innerchr9:137938480..137939553hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg381074
hg191074
hg181074
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1148266, nssv1148269, nssv1148267, nssv1148268
Samples
Known GenesCAMSAP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615936
Frequency
Sample Size17421
Observed Gain2
Observed Loss2
Observed Complex0
Frequencyn/a


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