A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007114



Internal ID19096332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:56076751..56189215hg38UCSC Ensembl
Innerchr4:56942917..57055381hg19UCSC Ensembl
Innerchr4:56637674..56750138hg18UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38112465
hg19112465
hg18112465
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5212n100
Supporting Variantsnssv3625283
Samples
Known GenesKIAA1211
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1007114
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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