A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170173



Internal ID21314234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:38646657..38648645hg38UCSC Ensembl
Outerchr2:38635081..38651175hg38UCSC Ensembl
Innerchr2:38873799..38875787hg19UCSC Ensembl
Outerchr2:38862223..38878317hg19UCSC Ensembl
Innerchr2:38727303..38729291hg18UCSC Ensembl
Outerchr2:38715727..38731821hg18UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg3816095
hg1916095
hg1816095
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14250115
SamplesMLY_9
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170173
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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