A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608995



Internal ID16049718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:150856387..150875294hg38UCSC Ensembl
Innerchr7:150553475..150572382hg19UCSC Ensembl
Innerchr7:150184408..150203315hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3818908
hg1918908
hg1818908
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11719n54
Supporting Variantsnssv1099489, nssv1099485, nssv1099486, nssv1099488, nssv1099487
Samples
Known GenesAOC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608995
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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