A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617993



Internal ID20991064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:116899601..116900400hg38UCSC Ensembl
chr7:116539655..116540454hg19UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18148604
Samples
Known GenesCAPZA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617993
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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