A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701896



Internal ID15091862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:248159177..248333561hg38UCSC Ensembl
Innerchr1:248322479..248496863hg19UCSC Ensembl
Innerchr1:246389102..246563486hg18UCSC Ensembl
Innerchr1:244648520..244822904hg17UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg38174385
hg19174385
hg18174385
hg17174385
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515858
Supporting Variants
Samples
Known GenesOR2M2, OR2M3, OR2M4, OR2M7, OR2T12, OR2T33
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701896
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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