A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696388



Internal ID15086354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162078145..162079152hg38UCSC Ensembl
Innerchr6:162499177..162500184hg19UCSC Ensembl
Innerchr6:162419167..162420174hg18UCSC Ensembl
Innerchr6:162469588..162470595hg17UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg381008
hg191008
hg181008
hg171008
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517562
Supporting Variants
Samples
Known GenesPARK2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696388
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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