A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615975



Internal ID16056698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:136605258..136676165hg38UCSC Ensembl
Innerchr9:139499710..139570617hg19UCSC Ensembl
Innerchr9:138619531..138690438hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3870908
hg1970908
hg1870908
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv13005n54
Supporting Variantsnssv1176161
SamplesNINDS_168
Known GenesAGPAT2, EGFL7, MIR126
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615975
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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