A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596226



Internal ID16036949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:173169007..173169959hg38UCSC Ensembl
Innerchr4:174090158..174091110hg19UCSC Ensembl
Innerchr4:174326733..174327685hg18UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg38953
hg19953
hg18953
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9397n54
Supporting Variantsnssv1016864
Samples
Known GenesGALNT7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596226
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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