A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1173100



Internal ID15855546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:106700640..106770988hg38UCSC Ensembl
Innerchr1:107243262..107313610hg19UCSC Ensembl
Innerchr1:107044785..107115133hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3870349
hg1970349
hg1870349
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv547328
Supporting Variants
Samples1782681096_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1173100
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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