A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6613268



Internal ID20986339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:75738194..75742127hg38UCSC Ensembl
chr7:75367512..75371445hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg383934
hg193934
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18158127
Samples
Known GenesHIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6613268
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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