A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169421



Internal ID21313904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:81018835..81028308hg38UCSC Ensembl
Outerchr4:81010103..81033509hg38UCSC Ensembl
Innerchr4:81939989..81949462hg19UCSC Ensembl
Outerchr4:81931257..81954663hg19UCSC Ensembl
Innerchr4:82159013..82168486hg18UCSC Ensembl
Outerchr4:82150281..82173687hg18UCSC Ensembl
Cytoband4q21.21
Allele length
AssemblyAllele length
hg3823407
hg1923407
hg1823407
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14245931, nssv14242262
SamplesMLY_7, NGO_11
Known GenesBMP3
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169421
Frequency
Sample Size93
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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