A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv778995



Internal ID16072951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:73596891..73597599hg38UCSC Ensembl
Innerchr11:73307936..73308644hg19UCSC Ensembl
Innerchr11:72985584..72986292hg18UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38709
hg19709
hg18709
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555412
Supporting Variants
Samples
Known GenesFAM168A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv778995
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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