A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1053824



Internal ID15907010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32017441..32022521hg38UCSC Ensembl
Innerchr6:31985218..31990298hg19UCSC Ensembl
Innerchr6:32093196..32098276hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg385081
hg195081
hg185081
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv602077
Supporting Variants
Samples
Known GenesC4A, C4B, C4B_2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1053824
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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