A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169957



Internal ID21314018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:76941965..76944420hg38UCSC Ensembl
Outerchr9:76939544..76951948hg38UCSC Ensembl
Innerchr9:79556881..79559336hg19UCSC Ensembl
Outerchr9:79554460..79566864hg19UCSC Ensembl
Innerchr9:78746701..78749156hg18UCSC Ensembl
Outerchr9:78744280..78756684hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3812405
hg1912405
hg1812405
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14248347, nssv14247403, nssv14250045, nssv14243751, nssv14244316, nssv14247627, nssv14246229, nssv14243268, nssv14243023, nssv14245457, nssv14244563, nssv14246246, nssv14246339, nssv14241367, nssv14247176, nssv14248463, nssv14249665
SamplesSNI_17, NGO_3, SNI_13, MLY_1, SNI_7, NGO_9, PML_1, MLY_16, SNI_9, SNI_1, NGO_2, NGO_6, SNI_3, NGO_1, SNI_15, NGO_7, SNI_4
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169957
Frequency
Sample Size93
Observed Gain1
Observed Loss16
Observed Complex0
Frequencyn/a


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