A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030966



Internal ID18773498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:22202641..22256152hg38UCSC Ensembl
Innerchr6:22202870..22256381hg19UCSC Ensembl
Innerchr6:22310849..22364360hg18UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3853512
hg1953512
hg1853512
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654825
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1030966
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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