A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015582



Internal ID18758116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:150270897..150588016hg38UCSC Ensembl
Innerchr7:149967986..150285104hg19UCSC Ensembl
Innerchr7:149598919..149916037hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38317120
hg19317119
hg18317119
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3674254
Samples
Known GenesACTR3C, GIMAP4, GIMAP7, GIMAP8, LINC00996, LOC728743, LRRC61, RARRES2, REPIN1, RNU6-33P, RNU6-34P, ZBED6CL, ZNF775
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015582
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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