A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608503



Internal ID16395912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:142040277..142088919hg38UCSC Ensembl
Innerchr7:141740077..141788719hg19UCSC Ensembl
Innerchr7:141386546..141435188hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3848643
hg1948643
hg1848643
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11627n54
Supporting Variantsnssv1156036
SamplesNINDS_22
Known GenesMGAM
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608503
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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