A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022594



Internal ID18765128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143728285..143773176hg38UCSC Ensembl
Innerchr7:143425378..143470269hg19UCSC Ensembl
Innerchr7:143056311..143101202hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3844892
hg1944892
hg1844892
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6708n100
Supporting Variantsnssv3670416
Samples
Known GenesCTAGE6, FAM115C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022594
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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