A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511870



Internal ID15504609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:32016002..32023803hg38UCSC Ensembl
Outerchr6:31983779..31991580hg19UCSC Ensembl
Outerchr6:32091757..32099558hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg387802
hg197802
hg187802
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv624402
Samples1
Known GenesC4A, C4B, C4B_2
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv511870
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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