A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703703



Internal ID15440355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:37381254..37439471hg38UCSC Ensembl
Innerchr20:36009657..36067873hg19UCSC Ensembl
Innerchr20:35443071..35501287hg18UCSC Ensembl
Innerchr20:35443071..35501287hg17UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3858218
hg1958217
hg1858217
hg1758217
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516343
Supporting Variants
Samples
Known GenesSRC
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703703
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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