A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1067643



Internal ID15920829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:88109247..88489275hg38UCSC Ensembl
Innerchr6:88818965..89198994hg19UCSC Ensembl
Innerchr6:88875684..89255713hg18UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38380029
hg19380030
hg18380030
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604120
Supporting Variants
Samples
Known GenesCNR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1067643
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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