A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1101690



Internal ID15954876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:158508696..158552000hg38UCSC Ensembl
Innerchr7:158301388..158344692hg19UCSC Ensembl
Innerchr7:157994149..158037453hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3843305
hg1943305
hg1843305
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv609359
Supporting Variants
Samples
Known GenesMIR595, PTPRN2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1101690
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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