A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18217605



Internal ID20784645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139447402..139455392hg38UCSC Ensembl
chr7:139132148..139140138hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg387991
hg197991
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6417321
Supporting Variants
Samples
Known GenesKLRG2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18217605
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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