A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615888



Internal ID16403297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135577826..135579700hg38UCSC Ensembl
Innerchr9:138469672..138471546hg19UCSC Ensembl
Innerchr9:137609493..137611367hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg381875
hg191875
hg181875
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1147144, nssv1147143, nssv1147142
Samples
Known GenesLOC100130954
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615888
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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