A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5913633



Internal ID22688849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:137005617..137007590hg38UCSC Ensembl
chr7:136690364..136692337hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg381974
hg191974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17434019
Samples
Known GenesCHRM2, LOC349160
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5913633
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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