A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1082845



Internal ID15936031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:39505188..39510237hg38UCSC Ensembl
Innerchr7:39544787..39549836hg19UCSC Ensembl
Innerchr7:39511312..39516361hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg385050
hg195050
hg185050
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv606678
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)nssv1082845
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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