A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606678



Internal ID16394087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:39505188..39510237hg38UCSC Ensembl
Innerchr7:39544787..39549836hg19UCSC Ensembl
Innerchr7:39511312..39516361hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg385050
hg195050
hg185050
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11284n54
Supporting Variantsnssv1082845, nssv1082846
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606678
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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