A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3661418



Internal ID18959699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:55537724..55569895hg38UCSC Ensembl
Innerchr7:55605417..55637588hg19UCSC Ensembl
Innerchr7:55572911..55605082hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3832172
hg1932172
hg1832172
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1022174
Supporting Variants
Samples
Known GenesVOPP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3661418
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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