A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3749046



Internal ID18700641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:26190088..26246556hg38UCSC Ensembl
Innerchr6:26190316..26246784hg19UCSC Ensembl
Innerchr6:26298295..26354763hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3856469
hg1956469
hg1856469
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1021294
Supporting Variants
Samples
Known GenesHIST1H1D, HIST1H2AD, HIST1H2AE, HIST1H2BF, HIST1H2BG, HIST1H3D, HIST1H3E, HIST1H4E, HIST1H4F
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3749046
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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