A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170287



Internal ID21314348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:74989408..74999394hg38UCSC Ensembl
Outerchr8:74986266..75005907hg38UCSC Ensembl
Innerchr8:75901643..75911629hg19UCSC Ensembl
Outerchr8:75898501..75918142hg19UCSC Ensembl
Innerchr8:76064198..76074184hg18UCSC Ensembl
Outerchr8:76061056..76080697hg18UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg3819642
hg1919642
hg1819642
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14242671
SamplesMLY_13
Known GenesCRISPLD1
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170287
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer