A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6616239



Internal ID20989310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:111276248..111594460hg38UCSC Ensembl
chr7:110916304..111234516hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38318213
hg19318213
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7056n223
Supporting Variantsnssv18149156
Samples
Known GenesIMMP2L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6616239
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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