A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169418



Internal ID21313901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:111573675..111575348hg38UCSC Ensembl
Outerchr5:111565528..111581474hg38UCSC Ensembl
Innerchr5:110909372..110911045hg19UCSC Ensembl
Outerchr5:110901226..110917171hg19UCSC Ensembl
Innerchr5:110937271..110938944hg18UCSC Ensembl
Outerchr5:110929125..110945070hg18UCSC Ensembl
Cytoband5q22.1
Allele length
AssemblyAllele length
hg3815947
hg1915946
hg1815946
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14244351, nssv14242876, nssv14244808, nssv14246975, nssv14245256, nssv14241215, nssv14242114, nssv14251844, nssv14250726, nssv14247803, nssv14252103, nssv14241477, nssv14249050, nssv14246504
SamplesSNI_8, SNI_7, NGO_29, PML_1, MLY_16, NGO_24, NGO_50, MLY_9, MLY_2, PML_4, NGO_1, NGO_49, NGO_8, SNI_4
Known GenesSTARD4-AS1
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169418
Frequency
Sample Size93
Observed Gain2
Observed Loss12
Observed Complex0
Frequencyn/a


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