A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6600557



Internal ID20973628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2765251..2767958hg38UCSC Ensembl
chr7:2804885..2807592hg19UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg382708
hg192708
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228715
Samples
Known GenesGNA12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6600557
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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