A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169449



Internal ID21313932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:78811345..78818857hg38UCSC Ensembl
Outerchr6:78810972..78821538hg38UCSC Ensembl
Innerchr6:79521062..79528574hg19UCSC Ensembl
Outerchr6:79520689..79531255hg19UCSC Ensembl
Innerchr6:79577781..79585293hg18UCSC Ensembl
Outerchr6:79577408..79587974hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3810567
hg1910567
hg1810567
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14243020, nssv14252373, nssv14249119, nssv14248513, nssv14242153, nssv14251088, nssv14242832, nssv14249592, nssv14243428, nssv14248426, nssv14251899, nssv14244682, nssv14249459, nssv14249254, nssv14248907
SamplesMLY_15, NGO_27, SNI_13, NGO_53, NGO_32, NGO_47, NGO_40, PML_2, NGO_25, NGO_6, NGO_52, SNI_5, NGO_49, NGO_51, SNI_4
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169449
Frequency
Sample Size93
Observed Gain1
Observed Loss14
Observed Complex0
Frequencyn/a


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