A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv687101



Internal ID15077067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:44262172..44268516hg38UCSC Ensembl
Innerchr11:44283722..44290066hg19UCSC Ensembl
Innerchr11:44240298..44246642hg18UCSC Ensembl
Innerchr11:44240298..44246642hg17UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg386345
hg196345
hg186345
hg176345
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517357
Supporting Variants
Samples
Known GenesALX4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv687101
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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