A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608956



Internal ID20982027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:56037164..56039025hg38UCSC Ensembl
chr7:56104857..56106718hg19UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg381862
hg191862
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18157148
Samples
Known GenesPSPH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608956
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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