A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012300



Internal ID19101518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:64783785..64820448hg38UCSC Ensembl
Innerchr4:65649503..65686166hg19UCSC Ensembl
Innerchr4:65332098..65368761hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3836664
hg1936664
hg1836664
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3625951
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)nsv1012300
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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