A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608951



Internal ID16396360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:147314549..147315362hg38UCSC Ensembl
Innerchr7:147011641..147012454hg19UCSC Ensembl
Innerchr7:146642574..146643387hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38814
hg19814
hg18814
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11705n54
Supporting Variantsnssv1098068, nssv1098064, nssv1098063, nssv1098065, nssv1098066, nssv1098069, nssv1098067, nssv1098062
Samples
Known GenesCNTNAP2, MIR548I4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608951
Frequency
Sample Size17421
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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