A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601947



Internal ID16042670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31817451..31829645hg38UCSC Ensembl
Innerchr6:31785228..31797422hg19UCSC Ensembl
Innerchr6:31893207..31905401hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3812195
hg1912195
hg1812195
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10462n54
Supporting Variantsnssv1053527, nssv1053528
Samples
Known GenesHSPA1A, HSPA1B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601947
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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