A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3630967



Internal ID18929248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:92632131..92701470hg38UCSC Ensembl
Innerchr4:93553282..93622621hg19UCSC Ensembl
Innerchr4:93772305..93841644hg18UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3869340
hg1969340
hg1869340
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv999973
Supporting Variants
Samples
Known GenesGRID2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3630967
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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