A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv685511



Internal ID15075477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:24056425..24081015hg38UCSC Ensembl
Innerchr14:24525634..24550224hg19UCSC Ensembl
Innerchr14:23595474..23620064hg18UCSC Ensembl
Innerchr14:23595474..23620064hg17UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3824591
hg1924591
hg1824591
hg1724591
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516023
Supporting Variants
Samples
Known GenesCPNE6, LRRC16B, NRL
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv685511
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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