A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169697



Internal ID21313508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:37426961..37428462hg38UCSC Ensembl
Outerchr7:37424365..37430681hg38UCSC Ensembl
Innerchr7:37466564..37468065hg19UCSC Ensembl
Outerchr7:37463968..37470284hg19UCSC Ensembl
Innerchr7:37433089..37434590hg18UCSC Ensembl
Outerchr7:37430493..37436809hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg386317
hg196317
hg186317
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14241780
SamplesNGO_1
Known GenesELMO1
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169697
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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