A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169535



Internal ID21313768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:195656271..195729177hg38UCSC Ensembl
Outerchr3:195559056..195730018hg38UCSC Ensembl
Innerchr3:195383142..195456048hg19UCSC Ensembl
Outerchr3:195285898..195456889hg19UCSC Ensembl
Innerchr3:196868323..196941719hg18UCSC Ensembl
Outerchr3:196767187..196942560hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38170963
hg19170992
hg18175374
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14248121, nssv14243595, nssv14249611, nssv14244609
SamplesMLY_15, NGO_6, NGO_23, SNI_5
Known GenesAPOD, MIR570, MUC20, SDHAP2
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169535
Frequency
Sample Size93
Observed Gain1
Observed Loss3
Observed Complex0
Frequencyn/a


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