A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017872



Internal ID18760405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143521753..143701114hg38UCSC Ensembl
Innerchr7:143218846..143398207hg19UCSC Ensembl
Innerchr7:142928968..143029140hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38179362
hg19179362
hg18100173
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6699n100
Supporting Variantsnssv3754682
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)nsv1017872
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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