A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1077606



Internal ID15584106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:123956..197267hg38UCSC Ensembl
Innerchr7:123956..197267hg19UCSC Ensembl
Innerchr7:219039..292350hg18UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3873312
hg1973312
hg1873312
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605598
Supporting Variants
Samples
Known GenesFAM20C, LOC100507642
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1077606
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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