A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015431



Internal ID18757965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143846746..143897882hg38UCSC Ensembl
Innerchr7:143543839..143594975hg19UCSC Ensembl
Innerchr7:143174772..143225908hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3851137
hg1951137
hg1851137
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6724n100
Supporting Variantsnssv3671149
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)nsv1015431
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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