A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4009652



Internal ID22071283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:25266637..25335514hg38UCSC Ensembl
Outerchr1:25256850..25335721hg38UCSC Ensembl
Innerchr1:25593128..25662005hg19UCSC Ensembl
Outerchr1:25583341..25662212hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3878872
hg1978872
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155376
Supporting Variants
Samples
Known GenesRHD
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4009652
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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