A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17437974



Internal ID22495844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:76477100..76975148hg38UCSC Ensembl
chr7:76106417..76604465hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38498049
hg19498049
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5924813
Supporting Variants
Samples
Known GenesDTX2, LOC100133091, POMZP3, UPK3B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17437974
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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