A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606521



Internal ID16047244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:30919387..30922522hg38UCSC Ensembl
Innerchr7:30959002..30962137hg19UCSC Ensembl
Innerchr7:30925527..30928662hg18UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg383136
hg193136
hg183136
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1081798
Samples
Known GenesAQP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606521
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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