A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702403



Internal ID15439055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:51974681..51982666hg38UCSC Ensembl
Innerchr15:52266878..52274863hg19UCSC Ensembl
Innerchr15:50054170..50062155hg18UCSC Ensembl
Innerchr15:50054170..50062155hg17UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg387986
hg197986
hg187986
hg177986
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517399
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702403
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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