A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017057



Internal ID18759592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:27777998..27821905hg38UCSC Ensembl
Innerchr6:27745777..27789683hg19UCSC Ensembl
Innerchr6:27853756..27897662hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3843908
hg1943907
hg1843907
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655763
Samples
Known GenesHIST1H2AI, HIST1H2AJ, HIST1H2BL, HIST1H2BM, HIST1H3H
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017057
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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