A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153622



Internal ID15877652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:7868633..7906906hg38UCSC Ensembl
Innerchr6:7868866..7907139hg19UCSC Ensembl
Innerchr6:7813865..7852138hg18UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg3838274
hg1938274
hg1838274
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv600925
Supporting Variants
SamplesHGDP01023
Known GenesBLOC1S5-TXNDC5, BMP6, TXNDC5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153622
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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