A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3749045



Internal ID19047326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:26027180..26066853hg38UCSC Ensembl
Innerchr6:26027408..26067081hg19UCSC Ensembl
Innerchr6:26135387..26175060hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3839674
hg1939674
hg1839674
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1026692
Supporting Variants
Samples
Known GenesHIST1H1C, HIST1H2AB, HIST1H2BB, HIST1H3B, HIST1H3C, HIST1H4B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3749045
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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