A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14243516



Internal ID21304587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:34859961..34872874hg38UCSC Ensembl
Outerchr7:34855738..34875294hg38UCSC Ensembl
Innerchr7:34899573..34912486hg19UCSC Ensembl
Outerchr7:34895350..34914906hg19UCSC Ensembl
Innerchr7:34866098..34879011hg18UCSC Ensembl
Outerchr7:34861875..34881431hg18UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3819557
hg1919557
hg1819557
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169726
Supporting Variants
SamplesNGO_14
Known GenesNPSR1
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14243516
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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