A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14251099



Internal ID21313009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:76840593..77065145hg38UCSC Ensembl
Outerchr6:76839630..77079117hg38UCSC Ensembl
Innerchr6:77550310..77774862hg19UCSC Ensembl
Outerchr6:77549347..77788834hg19UCSC Ensembl
Innerchr6:77607029..77831581hg18UCSC Ensembl
Outerchr6:77606066..77845553hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38239488
hg19239488
hg18239488
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169613
Supporting Variants
SamplesSNI_6
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14251099
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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