A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617260



Internal ID20990331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:100396053..100396584hg38UCSC Ensembl
chr7:99993676..99994207hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38532
hg19532
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18147707
Samples
Known GenesPILRA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617260
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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