A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169777



Internal ID21313588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:41372886..41401814hg38UCSC Ensembl
Outerchr17:41371357..41403287hg38UCSC Ensembl
Innerchr17:39529138..39558066hg19UCSC Ensembl
Outerchr17:39527609..39559539hg19UCSC Ensembl
Innerchr17:36782664..36811592hg18UCSC Ensembl
Outerchr17:36781135..36813065hg18UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3831931
hg1931931
hg1831931
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14241606, nssv14246961
SamplesNGO_20, NGO_25
Known GenesKRT31, KRT34, LOC100505782
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169777
Frequency
Sample Size93
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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