A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14245931



Internal ID21304214
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 Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169421
Supporting Variants
SamplesNGO_11
Known GenesBMP3
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14245931
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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