A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1155387



Internal ID15508672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:114281072..114358191hg38UCSC Ensembl
Innerchr7:113921127..113998246hg19UCSC Ensembl
Innerchr7:113708363..113785482hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3877120
hg1977120
hg1877120
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv608232
Supporting Variants
Samples1780862574_A
Known GenesFOXP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1155387
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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