A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv624402



Internal ID15501252
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 StatusS
Merged Variantsnsv511870
Supporting Variants
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)nssv624402
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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