A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17429704



Internal ID22487574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:122073928..122074102hg38UCSC Ensembl
chr7:121713982..121714156hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg38175
hg19175
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5909902
Supporting Variants
Samples
Known GenesAASS
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17429704
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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