A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016798



Internal ID18759333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143846746..143913658hg38UCSC Ensembl
Innerchr7:143543839..143610751hg19UCSC Ensembl
Innerchr7:143174772..143241684hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3866913
hg1966913
hg1866913
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6724n100
Supporting Variantsnssv3671150
Samples
Known GenesFAM115A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016798
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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