A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169600



Internal ID21313833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:76048529..76052548hg38UCSC Ensembl
Outerchr15:76042215..76056133hg38UCSC Ensembl
Innerchr15:76340870..76344889hg19UCSC Ensembl
Outerchr15:76334556..76348474hg19UCSC Ensembl
Innerchr15:74127925..74131944hg18UCSC Ensembl
Outerchr15:74121611..74135529hg18UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg3813919
hg1913919
hg1813919
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14244878, nssv14242044
SamplesNGO_1, NGO_38
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169600
Frequency
Sample Size93
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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