A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6616431



Internal ID20989502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:17856578..17857108hg38UCSC Ensembl
chr7:17896201..17896731hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38531
hg19531
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154761
Samples
Known GenesSNX13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6616431
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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