A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034764



Internal ID18777297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:144176284..144378413hg38UCSC Ensembl
Innerchr7:143873377..144075506hg19UCSC Ensembl
Innerchr7:143504310..143706439hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38202130
hg19202130
hg18202130
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6727n100
Supporting Variantsnssv3671170
Samples
Known GenesARHGEF34P, ARHGEF35, ARHGEF5, CTAGE4, CTAGE8, OR2A1, OR2A20P, OR2A42, OR2A7, OR2A9P, RNU6-57P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1034764
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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