A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170309



Internal ID21314370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:71080237..71082747hg38UCSC Ensembl
Outerchr4:71079443..71084739hg38UCSC Ensembl
Innerchr4:71945954..71948464hg19UCSC Ensembl
Outerchr4:71945160..71950456hg19UCSC Ensembl
Innerchr4:72164818..72167328hg18UCSC Ensembl
Outerchr4:72164024..72169320hg18UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg385297
hg195297
hg185297
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14243246, nssv14243025, nssv14243060
SamplesMLY_1, MLY_2, NGO_1
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170309
Frequency
Sample Size93
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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