A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14241606



Internal ID21305384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:41372886..41380422hg38UCSC Ensembl
Outerchr17:41371357..41391076hg38UCSC Ensembl
Innerchr17:39529138..39536674hg19UCSC Ensembl
Outerchr17:39527609..39547328hg19UCSC Ensembl
Innerchr17:36782664..36790200hg18UCSC Ensembl
Outerchr17:36781135..36800854hg18UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3819720
hg1919720
hg1819720
Variant TypeCNV duplication
Copy Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169777
Supporting Variants
SamplesNGO_20
Known GenesKRT34
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14241606
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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