A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14243965



Internal ID21301707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:10067773..10069647hg38UCSC Ensembl
Outerchr6:10067770..10072210hg38UCSC Ensembl
Innerchr6:10068006..10069880hg19UCSC Ensembl
Outerchr6:10068003..10072443hg19UCSC Ensembl
Innerchr6:10175992..10177866hg18UCSC Ensembl
Outerchr6:10175989..10180429hg18UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg384441
hg194441
hg184441
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169400
Supporting Variants
SamplesMLY_1
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14243965
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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