A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006981



Internal ID19096199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:17643727..17728912hg38UCSC Ensembl
Innerchr4:17645350..17730535hg19UCSC Ensembl
Innerchr4:17254448..17339633hg18UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3885186
hg1985186
hg1885186
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3737703
Samples
Known GenesFAM184B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1006981
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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