A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026280



Internal ID19115497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143514550..143850167hg38UCSC Ensembl
Innerchr7:143211643..143547260hg19UCSC Ensembl
Innerchr7:142921765..143178193hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38335618
hg19335618
hg18256429
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6702n100
Supporting Variantsnssv3669669
Samples
Known GenesCTAGE15, CTAGE6, EPHA1-AS1, FAM115C, LOC154761
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026280
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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