A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1078353



Internal ID15584853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:1388817..1541285hg38UCSC Ensembl
Innerchr7:1428453..1580921hg19UCSC Ensembl
Innerchr7:1394979..1547447hg18UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38152469
hg19152469
hg18152469
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605814
Supporting Variants
Samples
Known GenesINTS1, MAFK, MICALL2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1078353
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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