A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017203



Internal ID18759738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143512758..143701114hg38UCSC Ensembl
Innerchr7:143209851..143398207hg19UCSC Ensembl
Innerchr7:142919973..143029140hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38188357
hg19188357
hg18109168
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6699n100
Supporting Variantsnssv3669652
Samples
Known GenesCTAGE15, EPHA1-AS1, FAM115C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017203
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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