A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1081784



Internal ID15934970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:30755672..30801825hg38UCSC Ensembl
Innerchr7:30795288..30841441hg19UCSC Ensembl
Innerchr7:30761813..30807966hg18UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3846154
hg1946154
hg1846154
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv606507
Supporting Variants
Samples
Known GenesFAM188B, INMT, INMT-FAM188B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1081784
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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