A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170018



Internal ID21314079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:8428649..8441545hg38UCSC Ensembl
Outerchr2:8427502..8443948hg38UCSC Ensembl
Innerchr2:8568779..8581675hg19UCSC Ensembl
Outerchr2:8567632..8584078hg19UCSC Ensembl
Innerchr2:8486230..8499126hg18UCSC Ensembl
Outerchr2:8485083..8501529hg18UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3816447
hg1916447
hg1816447
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14244077
SamplesMLY_9
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170018
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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