A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007924



Internal ID19097143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:115317573..115477222hg38UCSC Ensembl
Innerchr4:116238729..116398378hg19UCSC Ensembl
Innerchr4:116458178..116617827hg18UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38159650
hg19159650
hg18159650
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3639327
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1007924
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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