A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703753



Internal ID15093719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:26372558..26379309hg38UCSC Ensembl
Innerchr6:26372786..26379537hg19UCSC Ensembl
Innerchr6:26480765..26487516hg18UCSC Ensembl
Innerchr6:26480765..26487516hg17UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg386752
hg196752
hg186752
hg176752
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527328
Supporting Variants
Samples
Known GenesBTN3A2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703753
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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