A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527699



Internal ID15454992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:210656104..210656976hg38UCSC Ensembl
Innerchr1:210829448..210830320hg19UCSC Ensembl
Innerchr1:208896071..208896943hg18UCSC Ensembl
Innerchr1:207217843..207218715hg17UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg38873
hg19873
hg18873
hg17873
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704177
Samples
Known GenesHHAT
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527699
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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