A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705442



Internal ID15095408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:17184523..17199629hg38UCSC Ensembl
Innerchr22:17665413..17680519hg19UCSC Ensembl
Innerchr22:16045413..16060519hg18UCSC Ensembl
Innerchr22:16039967..16055073hg17UCSC Ensembl
Cytoband22q11.1
Allele length
AssemblyAllele length
hg3815107
hg1915107
hg1815107
hg1715107
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528777
Supporting Variants
Samples
Known GenesCECR1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705442
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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