A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697885



Internal ID15087851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:43371080..43376550hg38UCSC Ensembl
Innerchr10:43866528..43871998hg19UCSC Ensembl
Innerchr10:43186534..43192004hg18UCSC Ensembl
Innerchr10:43186534..43192004hg17UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg385471
hg195471
hg185471
hg175471
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521283
Supporting Variants
Samples
Known GenesFXYD4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697885
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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