A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1154183



Internal ID15855361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:92238746..92263524hg38UCSC Ensembl
Innerchr6:92948464..92973242hg19UCSC Ensembl
Innerchr6:93005185..93029963hg18UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3824779
hg1924779
hg1824779
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604139
Supporting Variants
Samples1780862574_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1154183
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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