A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027593



Internal ID18770125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:159014422..159131365hg38UCSC Ensembl
Innerchr7:158807113..158924056hg19UCSC Ensembl
Innerchr7:158499874..158616817hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38116944
hg19116944
hg18116944
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3757754
Samples
Known GenesLINC00689, VIPR2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1027593
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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