A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022655



Internal ID18765189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143700937..143755783hg38UCSC Ensembl
Innerchr7:143398030..143452876hg19UCSC Ensembl
Innerchr7:143028963..143083809hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3854847
hg1954847
hg1854847
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3670411
Samples
Known GenesCTAGE6, FAM115C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022655
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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