A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv659097



Internal ID15395749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:189866390..189909464hg38UCSC Ensembl
Innerchr1:189835520..189878594hg19UCSC Ensembl
Innerchr1:188102143..188145217hg18UCSC Ensembl
Innerchr1:186567177..186610251hg17UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg3843075
hg1943075
hg1843075
hg1743075
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516072
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv659097
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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