A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17441358



Internal ID22499228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:128050589..128057955hg38UCSC Ensembl
chr7:127690641..127698007hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg387367
hg197367
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5927322
Supporting Variants
Samples
Known GenesSND1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17441358
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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