A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1016868



Internal ID15964138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:173169112..173169820hg38UCSC Ensembl
Innerchr4:174090263..174090971hg19UCSC Ensembl
Innerchr4:174326838..174327546hg18UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg38709
hg19709
hg18709
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv596229
Supporting Variants
Samples
Known GenesGALNT7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1016868
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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