A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17502062



Internal ID22560002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139477895..139481003hg38UCSC Ensembl
chr7:139162641..139165749hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg383109
hg193109
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5866889
Supporting Variants
Samples
Known GenesKLRG2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17502062
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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