A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607556



Internal ID16048279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:76035593..76048067hg38UCSC Ensembl
Innerchr7:75664911..75677385hg19UCSC Ensembl
Innerchr7:75502847..75515321hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3812475
hg1912475
hg1812475
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11459n54
Supporting Variantsnssv1087970
Samples
Known GenesMDH2, STYXL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607556
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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