A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703173



Internal ID15093139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:108823664..108834661hg38UCSC Ensembl
Innerchr1:109366286..109377283hg19UCSC Ensembl
Innerchr1:109167809..109178806hg18UCSC Ensembl
Innerchr1:109078328..109089325hg17UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3810998
hg1910998
hg1810998
hg1710998
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526819
Supporting Variants
Samples
Known GenesAKNAD1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703173
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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