A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155550



Internal ID22086055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:9163996..9167445hg38UCSC Ensembl
Outerchr19:9163124..9174084hg38UCSC Ensembl
Innerchr19:9274672..9278121hg19UCSC Ensembl
Outerchr19:9273800..9284760hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3810961
hg1910961
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4013441, nssv4013449, nssv4013443, nssv4013438, nssv4013436, nssv4013433, nssv4013440, nssv4013448, nssv4013444, nssv4013434, nssv4013451, nssv4013447, nssv4013435, nssv4013439, nssv4013445, nssv4013446, nssv4013442, nssv4013450
Samples
Known GenesZNF317
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155550
Frequency
Sample Size131
Observed Gain1
Observed Loss17
Observed Complex0
Frequencyn/a


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