A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606677



Internal ID16394086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:39505188..39509527hg38UCSC Ensembl
Innerchr7:39544787..39549126hg19UCSC Ensembl
Innerchr7:39511312..39515651hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg384340
hg194340
hg184340
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11284n54
Supporting Variantsnssv1082844
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606677
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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