A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18155286



Internal ID20722326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139675272..139675844hg38UCSC Ensembl
chr7:139360018..139360590hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38573
hg19573
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6421773
Supporting Variants
Samples
Known GenesHIPK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18155286
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00041


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