A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169976



Internal ID21314037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:16528801..16567351hg38UCSC Ensembl
Outerchr7:16525715..16571067hg38UCSC Ensembl
Innerchr7:16568426..16606976hg19UCSC Ensembl
Outerchr7:16565340..16610692hg19UCSC Ensembl
Innerchr7:16534951..16573501hg18UCSC Ensembl
Outerchr7:16531865..16577217hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3845353
hg1945353
hg1845353
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14244726
SamplesSNI_11
Known GenesLRRC72
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169976
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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