A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170000



Internal ID21314061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:120432212..120467056hg38UCSC Ensembl
Outerchr10:120430797..120475691hg38UCSC Ensembl
Innerchr10:122191724..122226568hg19UCSC Ensembl
Outerchr10:122190309..122235203hg19UCSC Ensembl
Innerchr10:122181714..122216558hg18UCSC Ensembl
Outerchr10:122180299..122225193hg18UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg3844895
hg1944895
hg1844895
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14251895
SamplesNGO_21
Known GenesPPAPDC1A
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170000
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