A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1100258



Internal ID15953444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:155234303..155281956hg38UCSC Ensembl
Innerchr7:155026013..155073666hg19UCSC Ensembl
Innerchr7:154656946..154704599hg18UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg3847654
hg1947654
hg1847654
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv609121
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1100258
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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