A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170176



Internal ID21314237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:214831225..214836633hg38UCSC Ensembl
Outerchr1:214820811..214837316hg38UCSC Ensembl
Innerchr1:215004568..215009976hg19UCSC Ensembl
Outerchr1:214994154..215010659hg19UCSC Ensembl
Innerchr1:213071191..213076599hg18UCSC Ensembl
Outerchr1:213060777..213077282hg18UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg3816506
hg1916506
hg1816506
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14247148
SamplesMLY_15
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170176
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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