A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595652



Internal ID16383061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:147006075..147041280hg38UCSC Ensembl
Innerchr4:147927227..147962432hg19UCSC Ensembl
Innerchr4:148146677..148181882hg18UCSC Ensembl
Cytoband4q31.22
Allele length
AssemblyAllele length
hg3835206
hg1935206
hg1835206
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152841
Samples1780854489_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595652
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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