A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606569



Internal ID16393978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:31550861..31552146hg38UCSC Ensembl
Innerchr7:31590475..31591760hg19UCSC Ensembl
Innerchr7:31557000..31558285hg18UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg381286
hg191286
hg181286
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11265n54
Supporting Variantsnssv1082518, nssv1082523, nssv1082519, nssv1082521, nssv1082525, nssv1082524, nssv1082520, nssv1082522
Samples
Known GenesCCDC129
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606569
Frequency
Sample Size17421
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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