A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1035095



Internal ID15541595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:74697056..74799717hg38UCSC Ensembl
Innerchr5:73992881..74095542hg19UCSC Ensembl
Innerchr5:74028637..74131298hg18UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg38102662
hg19102662
hg18102662
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv598653
Supporting Variants
Samples
Known GenesFAM169A, GFM2, HEXB, NSA2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1035095
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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