A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601946



Internal ID16042669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31814840..31827305hg38UCSC Ensembl
Innerchr6:31782617..31795082hg19UCSC Ensembl
Innerchr6:31890596..31903061hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3812466
hg1912466
hg1812466
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10462n54
Supporting Variantsnssv1053526
Samples
Known GenesHSPA1A, HSPA1L
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601946
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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