A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705222



Internal ID15095188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:206235962..206240576hg38UCSC Ensembl
Innerchr2:207100686..207105300hg19UCSC Ensembl
Innerchr2:206808931..206813545hg18UCSC Ensembl
Innerchr2:206926192..206930806hg17UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg384615
hg194615
hg184615
hg174615
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528596
Supporting Variants
Samples
Known GenesGPR1-AS
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705222
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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