A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6601074



Internal ID20974145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:17886982..17887557hg38UCSC Ensembl
chr7:17926605..17927180hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38576
hg19576
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229865
Samples
Known GenesSNX13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6601074
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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