A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170023



Internal ID21314084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:173728221..173732840hg38UCSC Ensembl
Outerchr2:173725212..173732928hg38UCSC Ensembl
Innerchr2:174592949..174597568hg19UCSC Ensembl
Outerchr2:174589940..174597656hg19UCSC Ensembl
Innerchr2:174301195..174305814hg18UCSC Ensembl
Outerchr2:174298186..174305902hg18UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg387717
hg197717
hg187717
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14244321
SamplesNGO_23
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170023
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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