A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170170



Internal ID21314231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:21693006..21721221hg38UCSC Ensembl
Outerchr11:21692916..21724212hg38UCSC Ensembl
Innerchr11:21714552..21742767hg19UCSC Ensembl
Outerchr11:21714462..21745758hg19UCSC Ensembl
Innerchr11:21671128..21699343hg18UCSC Ensembl
Outerchr11:21671038..21702334hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3831297
hg1931297
hg1831297
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14251055, nssv14248527
SamplesMLY_17, NGO_44
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170170
Frequency
Sample Size93
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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