A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527586



Internal ID15454879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:30963808..30964204hg38UCSC Ensembl
Innerchr7:31003423..31003819hg19UCSC Ensembl
Innerchr7:30969948..30970344hg18UCSC Ensembl
Innerchr7:30776663..30777059hg17UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg38397
hg19397
hg18397
hg17397
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704047
Samples
Known GenesGHRHR
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527586
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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