A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169895



Internal ID21313706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35358591..35379534hg38UCSC Ensembl
Outerchr19:35358420..35383481hg38UCSC Ensembl
Innerchr19:35849493..35870436hg19UCSC Ensembl
Outerchr19:35849322..35874383hg19UCSC Ensembl
Innerchr19:40541333..40562276hg18UCSC Ensembl
Outerchr19:40541162..40566223hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3825062
hg1925062
hg1825062
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14246927, nssv14243550, nssv14248160, nssv14248721, nssv14251239, nssv14251390, nssv14241419, nssv14246034, nssv14243618, nssv14242223, nssv14246845
SamplesSNI_17, NGO_3, MLY_6, MLY_5, MLY_11, MLY_12, NGO_29, NGO_10, PML_1, NGO_47, PML_4
Known GenesFFAR3
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169895
Frequency
Sample Size93
Observed Gain2
Observed Loss9
Observed Complex0
Frequencyn/a


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