A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596224



Internal ID16383633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:173169007..173169763hg38UCSC Ensembl
Innerchr4:174090158..174090914hg19UCSC Ensembl
Innerchr4:174326733..174327489hg18UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg38757
hg19757
hg18757
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1016862
Samples
Known GenesGALNT7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596224
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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