A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18212380



Internal ID20779420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:7586316..7837522hg38UCSC Ensembl
chr4:7588043..7839249hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38251207
hg19251207
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6371342
Supporting Variants
Samples
Known GenesAFAP1, AFAP1-AS1, SORCS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18212380
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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