A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156611



Internal ID22087012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:143541857..143764768hg38UCSC Ensembl
Outerchr1:143538619..143778901hg38UCSC Ensembl
Innerchr1:149036524..149259416hg19UCSC Ensembl
Outerchr1:149024808..149273545hg19UCSC Ensembl
Cytoband1q21.2
Allele length
AssemblyAllele length
hg38240283
hg19248738
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv18n97
Supporting Variantsnssv4021020, nssv4020522, nssv4020537, nssv4020529, nssv4020531, nssv4020527, nssv4021025, nssv4020533, nssv4021019, nssv4020526, nssv4021021, nssv4020532, nssv4021022, nssv4020523, nssv4020538, nssv4020525, nssv4021023, nssv4020530, nssv4020536, nssv4020524, nssv4020534, nssv4021024, nssv4020528, nssv4020535
Samples
Known GenesLOC101929780, NBPF23
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156611
Frequency
Sample Size131
Observed Gain0
Observed Loss24
Observed Complex0
Frequencyn/a


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