A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169465



Internal ID21313948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:34637053..34638890hg38UCSC Ensembl
Outerchr1:34626073..34648667hg38UCSC Ensembl
Innerchr1:35102654..35104491hg19UCSC Ensembl
Outerchr1:35091674..35114268hg19UCSC Ensembl
Innerchr1:34875241..34877078hg18UCSC Ensembl
Outerchr1:34864261..34886855hg18UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3822595
hg1922595
hg1822595
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14242233, nssv14245655, nssv14247083, nssv14244173, nssv14245909
SamplesNGO_18, NGO_53, NGO_19, NGO_49, NGO_34
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169465
Frequency
Sample Size93
Observed Gain1
Observed Loss4
Observed Complex0
Frequencyn/a


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