A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608973



Internal ID16049696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:148976273..149069299hg38UCSC Ensembl
Innerchr7:148673365..148766391hg19UCSC Ensembl
Innerchr7:148304298..148397324hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3893027
hg1993027
hg1893027
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1099466
Samples
Known GenesPDIA4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608973
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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