A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705369



Internal ID15442021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:126610956..126644710hg38UCSC Ensembl
Innerchr9:129373235..129406989hg19UCSC Ensembl
Innerchr9:128413056..128446810hg18UCSC Ensembl
Innerchr9:126452789..126486543hg17UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3833755
hg1933755
hg1833755
hg1733755
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528719
Supporting Variants
Samples
Known GenesLMX1B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705369
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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