A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6619534



Internal ID20992605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:39559101..39632800hg38UCSC Ensembl
chr7:39598700..39672399hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3873700
hg1973700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6653n223
Supporting Variantsnssv18225715
Samples
Known GenesRALA, YAE1D1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6619534
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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