A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17444231



Internal ID22502101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:27616317..27627404hg38UCSC Ensembl
chr7:27655936..27667023hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg3811088
hg1911088
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5925179
Supporting Variants
Samples
Known GenesHIBADH
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17444231
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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