A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14252532



Internal ID21311057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:4315439..4495166hg38UCSC Ensembl
Outerchr7:4311864..4500804hg38UCSC Ensembl
Innerchr7:4355070..4534797hg19UCSC Ensembl
Outerchr7:4351495..4540435hg19UCSC Ensembl
Innerchr7:4321596..4501323hg18UCSC Ensembl
Outerchr7:4318021..4506961hg18UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38188941
hg19188941
hg18188941
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169807
Supporting Variants
SamplesPML_3
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14252532
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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