A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607860



Internal ID16395269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:95336578..95347193hg38UCSC Ensembl
Innerchr7:94965890..94976505hg19UCSC Ensembl
Innerchr7:94803826..94814441hg18UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3810616
hg1910616
hg1810616
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11514n54
Supporting Variantsnssv1091193
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607860
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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