A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3633888



Internal ID18585483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:79291781..79591202hg38UCSC Ensembl
Innerchr4:80212935..80512356hg19UCSC Ensembl
Innerchr4:80431959..80731380hg18UCSC Ensembl
Cytoband4q21.21
Allele length
AssemblyAllele length
hg38299422
hg19299422
hg18299422
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv999174
Supporting Variants
Samples
Known GenesGK2, LINC00989, LINC01088, NAA11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3633888
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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