A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606679



Internal ID16394088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:39505188..39511421hg38UCSC Ensembl
Innerchr7:39544787..39551020hg19UCSC Ensembl
Innerchr7:39511312..39517545hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg386234
hg196234
hg186234
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11283n54
Supporting Variantsnssv1082847
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606679
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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