A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021242



Internal ID19110460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:142867307..142879931hg38UCSC Ensembl
Innerchr4:143788460..143801084hg19UCSC Ensembl
Innerchr4:144007910..144020534hg18UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg3812625
hg1912625
hg1812625
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5410n100
Supporting Variantsnssv3641194
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)nsv1021242
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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