A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017201



Internal ID18759736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:150955242..150965252hg38UCSC Ensembl
Innerchr4:151876394..151886404hg19UCSC Ensembl
Innerchr4:152095844..152105854hg18UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3810011
hg1910011
hg1810011
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3636092
Samples
Known GenesLRBA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017201
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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