A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3754834



Internal ID19053115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:144172363..144354126hg38UCSC Ensembl
Innerchr7:143869456..144051219hg19UCSC Ensembl
Innerchr7:143500389..143682152hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38181764
hg19181764
hg18181764
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1027780
Supporting Variants
Samples
Known GenesARHGEF34P, ARHGEF35, 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)nssv3754834
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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