A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006026



Internal ID18748557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:78111837..79966019hg38UCSC Ensembl
Innerchr4:79032991..80887173hg19UCSC Ensembl
Innerchr4:79252015..81106197hg18UCSC Ensembl
Cytoband4q21.21
Allele length
AssemblyAllele length
hg381854183
hg191854183
hg181854183
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3633881
Samples
Known GenesANTXR2, ANXA3, BMP2K, FRAS1, GK2, LINC00989, LINC01088, LINC01094, NAA11, PAQR3, PCAT4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1006026
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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