A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703710



Internal ID15440362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15002863..15002966hg38UCSC Ensembl
Innerchr19:15113675..15113778hg19UCSC Ensembl
Innerchr19:14974675..14974778hg18UCSC Ensembl
Innerchr19:14974675..14974778hg17UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg38104
hg19104
hg18104
hg17104
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527295
Supporting Variants
Samples
Known GenesSLC1A6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703710
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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