A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1087970



Internal ID15594470
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 StatusS
Merged Variantsnsv607556
Supporting Variants
Samples
Known GenesMDH2, STYXL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1087970
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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