A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6605722



Internal ID20978793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:20464997..21049074hg38UCSC Ensembl
chr7:20504620..21088693hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38584078
hg19584074
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236946
Samples
Known GenesABCB5, RPL23P8, SP8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6605722
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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