A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155376



Internal ID22085881
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 Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8n97
Supporting Variantsnssv4009844, nssv4012201, nssv4007276, nssv4009656, nssv4009653, nssv4007074, nssv4009660, nssv4012202, nssv4009659, nssv4009608, nssv4008377, nssv4007174, nssv4012205, nssv4010874, nssv4009654, nssv4008478, nssv4012200, nssv4012206, nssv4011076, nssv4012208, nssv4009658, nssv4012204, nssv4009662, nssv4012198, nssv4009650, nssv4009657, nssv4008579, nssv4010975, nssv4009663, nssv4012207, nssv4009652, nssv4012135, nssv4009743, nssv4012197, nssv4009661, nssv4009651, nssv4012199
Samples
Known GenesRHD
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155376
Frequency
Sample Size131
Observed Gain0
Observed Loss37
Observed Complex0
Frequencyn/a


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