A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608685



Internal ID16396094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143728268..143740341hg38UCSC Ensembl
Innerchr7:143425361..143437434hg19UCSC Ensembl
Innerchr7:143056294..143068367hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3812074
hg1912074
hg1812074
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1096535
Samples
Known GenesFAM115C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608685
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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