A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601320



Internal ID16042043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29891740..29927334hg38UCSC Ensembl
Innerchr6:29859517..29895111hg19UCSC Ensembl
Innerchr6:29967496..30003090hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3835595
hg1935595
hg1835595
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10348n54
Supporting Variantsnssv1051941
Samples
Known GenesHCG4B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601320
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer