A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6611794



Internal ID20984865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:111209634..111447510hg38UCSC Ensembl
chr7:110849690..111087566hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38237877
hg19237877
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7052n223
Supporting Variantsnssv18149126
Samples
Known GenesIMMP2L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6611794
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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