A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17436814



Internal ID22494684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:26331769..26344208hg38UCSC Ensembl
chr7:26371389..26383828hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg3812440
hg1912440
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5909256
Supporting Variants
Samples
Known GenesSNX10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17436814
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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