A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016605



Internal ID18759140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:144199147..144409403hg38UCSC Ensembl
Innerchr7:143896240..144106496hg19UCSC Ensembl
Innerchr7:143527173..143737429hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38210257
hg19210257
hg18210257
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6727n100
Supporting Variantsnssv3672458
Samples
Known GenesARHGEF34P, ARHGEF5, CTAGE4, CTAGE8, NOBOX, 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)nsv1016605
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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