A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1057874



Internal ID15564374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:34235629..34249404hg38UCSC Ensembl
Innerchr6:34203406..34217181hg19UCSC Ensembl
Innerchr6:34311384..34325159hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3813776
hg1913776
hg1813776
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv602865
Supporting Variants
Samples
Known GenesC6orf1, HMGA1, MIR6835
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1057874
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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