A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028886



Internal ID18771418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143521753..143875193hg38UCSC Ensembl
Innerchr7:143218846..143572286hg19UCSC Ensembl
Innerchr7:142928968..143203219hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38353441
hg19353441
hg18274252
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6706n100
Supporting Variantsnssv3754690
Samples
Known GenesCTAGE15, CTAGE6, EPHA1-AS1, FAM115A, 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)nsv1028886
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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