A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17441908



Internal ID22499778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:21489894..21508569hg38UCSC Ensembl
chr7:21529512..21548187hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3818676
hg1918676
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5918577
Supporting Variants
Samples
Known GenesSP4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17441908
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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