A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605871



Internal ID16046594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:2665632..2705490hg38UCSC Ensembl
Innerchr7:2705266..2745124hg19UCSC Ensembl
Innerchr7:2671792..2711650hg18UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg3839859
hg1939859
hg1839859
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1155116
SamplesNINDS_111
Known GenesAMZ1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605871
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer