A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170267



Internal ID21314328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:9163996..9167445hg38UCSC Ensembl
Outerchr19:9163124..9174084hg38UCSC Ensembl
Innerchr19:9274672..9278121hg19UCSC Ensembl
Outerchr19:9273800..9284760hg19UCSC Ensembl
Innerchr19:9135672..9139121hg18UCSC Ensembl
Outerchr19:9134800..9145760hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3810961
hg1910961
hg1810961
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14247474, nssv14248952, nssv14244126, nssv14251130, nssv14250447, nssv14248398, nssv14242688, nssv14248338, nssv14252158, nssv14249241, nssv14245455, nssv14246301, nssv14243940, nssv14242144, nssv14245864
SamplesMLY_6, SNI_8, NGO_32, NGO_45, NGO_4, NGO_47, NGO_6, PML_4, NGO_36, SNI_5, NGO_5, SNI_14, NGO_11, NGO_15, SNI_4
Known GenesZNF317
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170267
Frequency
Sample Size93
Observed Gain1
Observed Loss14
Observed Complex0
Frequencyn/a


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