A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029124



Internal ID18771656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:26857689..27141995hg38UCSC Ensembl
Innerchr6:26825468..27109774hg19UCSC Ensembl
Innerchr6:26933447..27217753hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38284307
hg19284307
hg18284307
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655756
Samples
Known GenesGUSBP2, HIST1H2AG, HIST1H2BJ, HIST1H2BK, HIST1H4I, LINC00240, LOC100270746
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029124
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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