A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015539



Internal ID19104756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:144199147..144378798hg38UCSC Ensembl
Innerchr7:143896240..144075891hg19UCSC Ensembl
Innerchr7:143527173..143706824hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38179652
hg19179652
hg18179652
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6735n100
Supporting Variantsnssv3672453, nssv3672452, nssv3756112, nssv3756111
Samples
Known GenesARHGEF34P, 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)nsv1015539
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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