A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6619441



Internal ID20992512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:124747012..124889814hg38UCSC Ensembl
chr7:124387066..124529868hg19UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg38142803
hg19142803
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232123
Samples
Known GenesGPR37, LOC154872, POT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6619441
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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