A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517806



Internal ID15445099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:139109872..139117415hg38UCSC Ensembl
Innerchr7:138794618..138802161hg19UCSC Ensembl
Innerchr7:138445158..138452701hg18UCSC Ensembl
Innerchr7:138251873..138259416hg17UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg387544
hg197544
hg187544
hg177544
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695210
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517806
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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