A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14251279



Internal ID21302153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:73290632..73298260hg38UCSC Ensembl
Outerchr6:73288278..73309615hg38UCSC Ensembl
Innerchr6:74000355..74007983hg19UCSC Ensembl
Outerchr6:73998001..74019338hg19UCSC Ensembl
Innerchr6:74057076..74064704hg18UCSC Ensembl
Outerchr6:74054722..74076059hg18UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3821338
hg1921338
hg1821338
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169710
Supporting Variants
SamplesMLY_12
Known GenesC6orf147, KHDC1
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14251279
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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