A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001793



Internal ID19091010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:141044..256048hg38UCSC Ensembl
Innerchr4:134825..249837hg19UCSC Ensembl
Innerchr4:124825..239837hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38115005
hg19115013
hg18115013
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5074n100
Supporting Variantsnssv3616071
Samples
Known GenesZNF718, ZNF876P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1001793
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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